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ccrpsorg · 1 year

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Good Pharmacovigilance Practice

Good Pharmacovigilance Practice Modules: A Comprehensive Guide to EMA GVP Modules

Good pharmacovigilance practices are the best way to ensure the safe and effective use of medicines. The European Medicines Agency (EMA) has set out a number of guidelines to ensure that all medicines are monitored safely and securely throughout their life cycle. You can review and become certified in these modules through our pharmacovigilance training program which is the only IAOCR-recognized program now taken by over 6,000 students.

Good pharmacovigilance practice PDF

In line with international standards, good pharmacovigilance practices require that companies or marketing authorization holders (MAHs) have an appropriate system in place to monitor the safety of medicines, collect data on potential risks and report any suspected adverse reactions. It is important for MAHs to be able to identify any potential safety issues quickly and take action when necessary.

In addition, EMA's Risk Management Plans provide further guidance on how companies should manage any risks associated with their products across the entire product lifecycle. These plans cover topics such as risk minimisation measures, benefit-risk assessment methods, additional monitoring systems and post-marketing studies.

It is essential that all pharmaceutical companies comply with good pharmacovigilance practices in order to ensure patient safety and quality medicines reach patients without unnecessary risks or delays. Following best practice guidelines helps protect public health by allowing for rapid detection of safety signals before serious harm can occur.

1.Pharmacovigilance Systems

The Guideline on Good Pharmacovigilance Practices (GVP) Module I – Pharmacovigilance Systems and Their Quality Systems outlines key principles, requirements and expectations for managing effective pharmacovigilance systems, as well as providing guidance on how to develop and maintain a quality system. The document provides a comprehensive overview of the regulatory framework and highlights the importance of an efficient, effective and compliant pharmacovigilance system. It includes information such as the definition of what constitutes a PV system, the role of relevant parties in setting up and operating such a system, expectations regarding PV processes and procedures, criteria for evaluating adequacy of PV systems, risk management activities, safety data exchange agreements and safety reporting procedures.

The document outlines the responsibilities associated with setting up a PV system and maintaining its quality assurance program. This includes ensuring that applicable laws or regulations are followed; obtaining the necessary resources (people, equipment); identifying appropriate roles for personnel involved in PV activities; developing policies, procedures and standards; monitoring performance; making sure that any changes to the system are properly validated/re-validated; implementing risk management plans; establishing an internal audit program; performing regular internal audits to ensure compliance with applicable laws or regulations; interacting with external organizations involved in safety surveillance activities. Additionally, it discusses topics such as data protection requirements, individual case safety report reconciliation processes, periodic safety update reports (PSURs), risk management plans (RMPs), signal detection methods and other related topics.

Overall this guideline is an essential reference tool for industry professionals responsible for setting up or maintaining pharmacovigilance systems. It provides a detailed description of all aspects relating to pharmacovigilance systems including those related to regulatory requirements, quality assurance programs and data protection measures. This makes it an ideal source of information for industry professionals looking to stay informed about best practices in this field.

2. Pharmacovigilance System Master File

The Guideline on Good Pharmacovigilance Practices (GVP) Module II – Pharmacovigilance System Master File (Rev 2) is a comprehensive document that outlines the best practices for companies involved in the pharmaceutical industry to ensure the safe use of their products. The document covers topics such as the required contents of a pharmacovigilance system master file (PSMF), recommendations for setting up, running and maintaining a PSMF, as well as safety-related responsibilities for healthcare professionals and companies.

The GVP Module II provides clear guidance on what should be included in the PSMF, including elements such as organizational information, operational processes, safety data management and reporting, safety risk management and analysis, and communication processes. It also outlines good practices related to quality assurance such as validation of data entry systems and implementation of change control procedures. Moreover, it provides detailed instructions related to specific roles within a pharmacovigilance system such as medical advisors, clinical evaluation experts and signal detection staff.

In addition to providing recommendations on how to implement adequate pharmacovigilance systems, this guideline also includes discussion points on how companies can validate their own individual systems. This includes guidance on how to audit against established standards such as those outlined by the European Medicines Agency (EMA). Furthermore, it outlines requirements for drug development plans including preclinical studies, clinical trials, post-authorization studies and post-marketing surveillance programs.

Overall, this document is an invaluable resource for anyone involved in any aspect of drug safety or pharmacovigilance. It provides clear guidance about what constitutes an adequate pharmacovigilance system for both healthcare professionals and companies involved in the pharmaceutical industry. Its detailed descriptions make it easy to understand exactly what needs to be done from concept through implementation and operation of a PSMF. Additionally its discussion points provide valuable insights into how existing systems may be evaluated or improved upon if needed.

3. Pharmacovigilance Inspections

The Guideline on Good Pharmacovigilance Practices (GVP) Module III – Pharmacovigilance Inspections (Rev 1) provides an overview of the inspection process and methodology used in pharmacovigilance. This document is intended to standardize the approach taken by authorities when carrying out inspections as part of their pharmacovigilance activities. The document starts by providing an overview of the objectives and scope of inspections, as well as a list of key elements that should be assessed during such inspections. It then goes on to outline the organization and conduct of inspections, including the roles and responsibilities of all those involved, before concluding with a discussion of post-inspection activities.

The document contains information on how to prepare for an inspection, including identifying risks, developing a detailed plan and appointing appropriately qualified inspectors. It also covers topics such as evidence gathering, reporting requirements, defining corrective and preventive actions (CAPA), handling disagreements between authorities and documentation requirements. The document also includes guidance on how to manage conflicts of interest during inspections, assess data integrity issues in clinical studies or establish a dialogue between authorities and inspected companies.

Overall, this guideline provides comprehensive information about conducting pharmacovigilance inspections. It sets out detailed instructions for all stages of such inspections – from preparing for them to taking corrective actions afterwards – helping ensure that these activities are carried out in a consistent manner across different countries. As such, this guideline is likely to be beneficial for both authorities responsible for managing safety concerns related to medicines and inspected companies which must comply with relevant regulations.

4. Pharmacovigilance Audits

The Guideline on Good Pharmacovigilance Practices (GVP) Module IV provides guidance for conducting pharmacovigilance audits. This document is intended to provide an overview of the essential elements of a robust quality system and auditor qualification, planning and preparation for the audit, conduct of the audit, closure and follow-up activities, and reporting.

The main objectives of conducting pharmacovigilance auditing are to ensure that the pharmacovigilance system meets applicable regulatory requirements and industry standards, while also promoting continuous improvement in safety management. The document outlines the expectations for planning and preparing for an audit including scope, criteria, documents to be reviewed, personnel to be interviewed and potential sources of evidence. It addresses important considerations such as effective communication with stakeholders during planning and performance of the audit.

The document also covers criteria to be used when selecting auditors to ensure objective assessments. Qualifications should include relevant knowledge within the area of pharmacovigilance as well as experience in conducting audits. Additionally, it specifies standards for verbal/written communications with all parties involved during an audit including respect for confidentiality/privacy requirements.

The document describes principles related to conducting the audit including appropriate documentation methods such as notes from witness interviews or observation forms. Guidelines are provided regarding evidence gathering techniques such as sample size determination, selection of subjects or records to review, duration of observations and additional topics related to ensuring effective data collection techniques are employed when necessary.

Additionally, this guideline outlines requirements for properly closing an audit including findings discussions with all parties involved followed by appropriate action plans that address any non-conformities found during the process. This action plan should aim at remediation of deficiencies found during either corrective or preventative actions if necessary/justified as well as a timeline for completion/follow-up actions on actions taken. Lastly, it describes expectations related to reporting post-audit activities which should include written reports addressing nonconformities found along with recommendations on corrective actions taken or additional preventive measures needed in order to ensure compliance with GVP guidelines going forward.

5. Risk Management Systems

The Guideline on Good Pharmacovigilance Practices (GVP) Module V- Risk Management Systems, revised for 2020, is a comprehensive document provided by the European Medicines Agency that outlines a framework for risk management systems of pharmaceutical products. It provides detailed guidance for manufacturers and marketing authorization holders during their production and distribution of medicinal products in Europe. The guideline covers topics such as the safety assessment process, risk minimization activities, communication of safety information to healthcare professionals and patients, pharmacovigilance audit procedures and training requirements.

The main aim of GVP Module V is to ensure that the risks associated with medicinal products are managed effectively throughout their lifecycle. This is achieved through an effective risk management system (RMS). To this end, the GVP sets out five core principles that should be adhered to when designing and implementing an RMS: monitoring and evaluation of safety information; risk minimization strategies; communication of safety information; audit and inspection; and training requirements.

Each principle is then broken down into more detailed elements which manufacturers/marketing authorization holders should consider when designing their RMS. These include: establishing objectives for the RMS; setting up a robust infrastructure to monitor safety data; developing risk minimization plans; communicating safety information to stakeholders on a regular basis; conducting audits/inspections on a regular basis; ensuring staff are trained appropriately in pharmacovigilance practices; setting up reporting systems to enable timely alerts if any significant new risks are identified; assessing performance metrics regularly to ensure processes remain effective over time.

6. Individual Case Safety Reports

The Guideline on good pharmacovigilance practices (GVP) Module VI provides guidance for companies and organizations in the collection and management of individual case safety reports (ICSRs) as well as their submission to regulatory authorities. The main purpose of this module is to ensure that pharmacovigilance activities are performed in a consistent and effective manner across the EU Member States, in order to protect public health, improve patient safety, and strengthen confidence in healthcare products.

The module covers topics such as process for ICSR collection, management, and submission process; risk management plan; responsibilities; quality control measures; data integrity requirements; monitoring of adverse events reporting systems; ICSR privacy considerations; electronic exchange of ICSRs between marketing authorization holders and national competent authorities; and post-marketing surveillance.

In addition to providing practical guidance on these topics, the module also outlines best practices for maintaining a comprehensive pharmacovigilance system. These include establishing an appropriate risk management plan for each authorized medicinal product, assigning roles and responsibilities appropriately, collecting timely ICSRs from all relevant sources (including spontaneous reports from healthcare professionals or patients), tracking safety signals on an ongoing basis, ensuring data integrity when exchanging ICSRs electronically with regulatory authorities, ensuring the security of personal data related to patients who report adverse reactions, and performing regular monitoring activities to assess compliance with pharmacovigilance obligations.

Overall, the Guideline on good pharmacovigilance practices (GVP) Module VI is a valuable resource for companies and organizations that seek to ensure that their pharmacovigilance operations are up-to-date with current regulations and standards. It provides useful information on how to develop an effective ICSR collection, management, and submission process while also emphasizing best practices for maintaining a comprehensive pharmacovigilance system that is compliant with applicable laws.

7. Period Safety Update Reports

The Guideline on good pharmacovigilance practices (GVP) Module VII is designed to provide guidance for the development and submission of periodic safety update reports (PSURs). This document provides information on the regulatory aspects, content and format for PSURs, as well as best practices for preparing and submitting them in accordance with the applicable risk management plan.

The GVP Module VII outlines the process needed to assess drug safety data from various sources, including spontaneous reports, clinical trials, epidemiological studies and post-authorization safety studies. It emphasizes that periodic safety reviews should be conducted at least annually and whenever new data suggests it is necessary. The main objective of a PSUR is to provide an assessment of the benefit-risk balance of a medicinal product over a defined period of time.

In order to ensure that all relevant data is accurately captured and tracked, the GVP Module VII recommends that companies maintain a comprehensive database containing both adverse event and non-adverse event information related to their products. This information should include any relevant clinical trial results or other relevant safety issues identified during pharmacovigilance activities. Additionally, the document outlines methods for evaluating reported events in order to identify potential safety signals.

Overall, Guideline on good pharmacovigilance practices (GVP) Module VII provides detailed guidance regarding the development and submission of periodic safety update reports (PSURs). It outlines processes for capturing, tracking, evaluating and assessing drug safety data from various sources. Furthermore, it discusses strategies for analyzing this data in order to identify potential safety signals which help inform regulatory decision making about a particular pharmaceutical product's risk-benefit balance over time.

8. Post Authorization Safety Studies

The Guideline on Good Pharmacovigilance Practices (GVP) Module VIII provides detailed guidance on the post-authorisation safety studies (PASS). This document is designed to help drug manufacturing companies, regulatory agencies and other stakeholders understand their respective roles and responsibilities in designing and conducting PASS.

The document outlines the principles of good pharmacovigilance practice and incorporates several international standards including those from the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH). The document also highlights the potential benefit of using available data sources such as Electronic Health Records and administrative healthcare databases, as well as patient registries.

In addition to general requirements related to PASS design, GVP Module VIII outlines specific requirements regarding patient eligibility criteria, study protocol adherence, sample size calculation and analysis, ethics/informed consent requirements, as well as specific reporting requirements.

The document contains clear instructions on how sponsors should prepare a detailed risk management plan (RMP) with respect to PASS. This includes outlining different types of safety monitoring procedures that should be conducted during a study. Furthermore, it provides guidance on providing adequate training to ensure appropriate execution of the RMP. Moreover, it outlines the importance of appropriately packaging and labelling test articles used in clinical trials to minimize any potential risks or harm associated with them.

Overall, GVP Module VIII provides comprehensive guidance for all stakeholders involved in Post-Authorisation Safety Studies by outlining clear roles and responsibilities as well assessing potential risks associated with these studies. It serves as an essential reference guide for manufacturers who wish to design effective PASS protocols that adhere to international standards in order to ensure patient safety while at the same time promoting innovation within the industry.

9. Signal Management

The Guideline on Good Pharmacovigilance Practices (GVP) Module IX on Signal Management is a comprehensive set of guidelines which provides the framework for the appropriate management of signals and safety issues related to medicines. It outlines the process for detecting and evaluating potential safety issues and risks associated with medicinal products, as well as providing guidance on when additional investigations should be considered, and how to respond when safety signals are identified. The document focusses on areas such as risk minimisation plans, benefit-risk assessments, laboratory tests, product recalls and market withdrawals.

The GVP Module IX begins by outlining the definitions and concepts associated with signal management. These include definitions of what a signal is, how a signal should be classified, when it is appropriate to consider further action and how to differentiate between pharmacovigilance activities and regulatory actions. This section also provides guidance on data sources which can be used to identify signals, including both spontaneous reports from healthcare professionals or consumers as well as epidemiological studies.

The next section details specific aspects of signal management such as risk minimisation activities, benefit-risk assessments, laboratory investigations and product recalls or market withdrawals. It outlines key points such as: planning risk minimisation strategies in advance; monitoring effectiveness; assessing the benefit-risk balance at regular intervals; conducting laboratory tests which are relevant to safety issues; recalling or withdrawing products where necessary; ensuring availability of up-to-date information about risks associated with medicines; considering other types of regulatory action where appropriate; maintaining records of all decisions made related to signal management; and reporting/publishing new information regarding any changes in risk assessment/benefit-risk balance.

Finally, GVP Module IX provides detailed guidance on post-marketing surveillance activities which should be conducted following implementation of any risk minimisation plans. This includes setting up systems for monitoring changes in safety profile after introduction into use in humans or in the environment, implementing quality control processes for data capture & analysis, garnering collaboration from stakeholders (e.g healthcare professionals & customer feedback), sharing data with other organisations/authorities where appropriate ,and implementing communication plans so that stakeholders are kept informed of any changes in risk assessment/benefit-risk balance due to new evidence becoming available over time.

10. Additional Drug Safety Monitoring

The Guideline on Good Pharmacovigilance Practices (GVP) Module on Additional Monitoring offers a comprehensive guide to the principles, methods and processes of additional monitoring in the field of pharmacovigilance. This document outlines the purpose, rationale and requirements of additional monitoring activities as well as providing practical guidance for its implementation. The module is divided into five sections: Introduction; Overview; Objectives; Policies and Procedures; and Resources and Tools. In addition, it provides detailed best practice recommendations for each of these subject areas.

The Introduction section offers an overview of pharmacovigilance as well as outlining the structure and purpose of GVP Module X on Additional Monitoring. It also provides definitions for key terms related to this area such as safety surveillance, signal detection, signal assessment, signal evaluation, risk management plan (RMP), post-marketing commitment (PMC) etc.

The Overview section provides a general overview of additional monitoring including an explanation of its objectives, purpose and importance in the management of drug safety risks. It goes on to discuss how additional monitoring data can be used by authorities to make informed decisions regarding marketing authorization or changes to an authorized product's RMP. The section also looks at how regulators can assess the adequacy of existing safety information and consider whether further data collection should be undertaken through additional monitoring activities.

The Objectives section outlines in detail the objectives to be fulfilled when undertaking additional monitoring activities such as obtaining further safety information about a marketed product or conducting ongoing risk-benefit assessments necessary for regulatory decision making about medicine availability or changes to an authorized product's RMP. It also discusses how appropriate target populations can be identified in order maximize benefit from the activity while minimizing risk from potential harms caused by inappropriate use or misuse of medicines.

The Policies and Procedures section explains in detail what should be included when developing procedures for implementing additional monitoring activities such as setting objectives for data collection, deciding target populations for data collection, identifying relevant sources of information (including electronic health records) etc. It also covers legal considerations such as patient consent requirements when collecting personal data through registries or other sources outside hospital settings etc., which are important when planning any form of clinical trial activity that uses anonymized patient data collected retrospectively from various sources (e.g., primary care centers).

Finally, the Resources and Tools section suggests some practical tools that may help with developing appropriate procedures when implementing additional monitoring activities such as questionnaires that could be used to collect patient reported outcome measures (PROMs) etc. In addition it outlines relevant international frameworks/agreements which must be taken into account when collecting global safety data sets through international registry networks such as those developed through ICH-GCP partnerships between different countries/regions across Europe or North America etc..

Overall this Guideline on Good Pharmacovigilance Practices Module X Additional Monitoring is an essential resource for anyone involved with designing or implementing pharmacovigiance systems since it provides comprehensive best practice advice that will help ensure safe use/distribution/monitoring of medicines worldwide

15. Pharmacovigilance Safety Communication

The Guideline on good pharmacovigilance practices (GVP) Module XV Safety Communication was developed to provide guidance to pharmaceutical companies and other healthcare stakeholders involved in the management of medicinal products. This document contains detailed instructions on how to effectively communicate risk related information about medicinal products.

The guidelines are designed to ensure that such communication is consistent, timely and accurate. It also highlights the importance of making sure that both healthcare professionals and patients have access to sufficient information so that they can make informed decisions about the medicine they are taking.

The document outlines a number of principles for effective safety communication, including: ensuring that all risk related information is identified and included in the communication; providing clear, accurate, up-to-date information; understanding who needs to be informed; responding quickly to questions raised by healthcare professionals; and making sure that patients have access to appropriate support after receiving information.

The guideline also sets out various requirements for monitoring and assessing the effectiveness of safety communications, including evaluating the impact of risk minimisation measures, collecting feedback from health professionals and consumers following safety communications, conducting surveys among healthcare professionals and monitoring changes in prescribing behaviour. The documentation also provides advice on dealing with adverse events associated with medicines as well as what steps should be taken when product recalls or withdrawals occur.

Overall, this Guideline on good pharmacovigilance practices (GVP) Module XV Safety Communication provides a comprehensive overview of best practices relating to safety communications concerning medicinal products. It provides specific advice on how pharmaceutical companies should communicate risk-related information about their medicines, as well as how to monitor the effectiveness of such communication. The guidance is invaluable for all stakeholders involved in managing medicinal products so that they can ensure patient safety is maintained at all times.

Want to understand good pharmacovigilance practice modules through examples, video lectures, and quizzes all while receiving The IAOCR internationally recognized certificate available for PV officers? Consider enrolling in CCRPS Pharmacovigilance certification.

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companysconnectsin · 1 year

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rhinoplasty-hyd · 5 years

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vovamayskiy · 6 years

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В Европе представлено пострегистрационное исследование российского оригинального препарата

Пострегистрационное исследование (PASS) российского оригинального препарата Полиоксидоний® в Европе представлено на международной конференции.

Уникальный для России проект многоцентрового открытого пострегистрационного исследования безопасности Post Authorisation Safety Study (PASS) инъекционной формы препарата Полиоксидоний® 6 мг в Европейском союзе (Словакия) представлен 15 ноября в рамках шестой международной конференции «Клинические исследования в России», организованной Институтом Адама Смита в Москве.

Российские фармацевтические компании все активнее развивают экспортное направление, и процесс проведения пострегистрационных клинических исследований в других странах становится одной из важных задач географической экспансии. Информации о том, что представляют собой пострегистрационные исследования безопасности (PASS) в ЕС, а также рассмотрению примера первого пострегистрационного исследования препарата Полиоксидоний® в Европе была посвящена отдельная сессия международной конференции.

Исследование было инициировано «НПО Петровакс Фарм» в 2015 году с целью дополнительного изучения профиля безопасности препарата в рутинной клинической практике. В 2017 году компания получила отчет о его успешных результатах, который подтвердил высокий профиль безопасности лекарственного средства и хорошую переносимость среди пациентов.

«Полиоксидоний® хорошо известен в России, странах СНГ, а также Словакии. Более 20 лет препарат успешно применяется в практическом здравоохранении 11 стран и заслужил доверие врачей и потребителей. За многие годы накоплен большой опыт клинических исследований лекарственного средства в России. И наш шаг в области проведения пострегистрационного исследования Полиоксидония® в Европе – это продолжение стратегии развития экспортного потенциала продукта за рубежом, в частности на территории Европейского союза. Это первый опыт пострегистрационных исследований российских препаратов в Европе в целом, который подтвердил высокую безопасность оригинального препарата, созданного российскими учеными, — отметила медицинский директор «НПО Петровакс Фарм» Наталья Чирун: — Пострегистрационные исследования безопасности относятся к лучшим практикам, которые приветствуются регуляторами Евросоюза. Для осуществления проекта наша компания привлекла контрактную исследовательскую организацию Биомапас, обладающую большим опытом проведения подобных исследований в ЕС».

«Проводя исследование препарата Полиоксидоний®, мы руководствовались обновленными требованиями стандарта ICH GVP Module VII (rev. 2) и ICH GCP, — продолжил управляющий директор компании Биомапас (Biomapas) Аудрюс Свейката. — Многоцентровое исследование PASS включало 502 взрослых пациента в 15 исследовательских центрах, которые были расположены по всей Словакии. Пациенты с показаниями «острые инфекции и хронические рецидивирующие заболевания вирусной и бактериальной этиологии» наблюдались в течение курса лечения, в среднем 22 дня. В финале исследования осуществлялась оценка общей переносимости лекарственного средства по мнению врачей-исследователей и пациентов. Результаты PASS показали, что Полиоксидоний® обладает высоким профилем безопасности и хорошо переносится исследуемой популяцией пациентов, — поделился данными спикер. — 75,3% пациентов и 79,7% исследователей оценили переносимость как очень хорошую, 21,1% пациентов и 19,3% исследователей — как хорошую».

Наталья Чирун обратила внимание на то, что PASS-исследование проводилось в соответствии с европейскими стандартами1 и было одобрено Регуляторным органом Словацкой Республики. Контроль клинических исследований осуществлялся в рамках Sponsor Oversight, все процедуры которого были строго регламентированы. Со стороны «НПО Петровакс Фарм» регулярно проводился мониторинг и аудит проекта в соответствии со стандартными операционными процедурами. Отчет об успешном окончании исследования войдет в состав регистрационного досье препарата для Словацкого регуляторного органа SUKL. Исследование зарегистрировано в Европейском регистре PASS2 и получило одобрение Европейского этического комитета. Этот опыт, безусловно, интересен для российской фармацевтической индустрии в рамках пострегистрационных исследований, заключила Наталья Чирун.

В чем особенность и преимущества PASS исследований по сравнению с рандомизированными клиническими исследованиями? Когда в России появятся регламенты, описывающие проведение таких исследований? – поднял вопросы в ходе дискуссии модератор сессии директор проектов Maxwell Biotech Group Дмитрий Мануилов.

«Основное преимущество PASS-исследований в том, что они помогают оценить выявленные, потенциальные или теоретические риски лекарственных препаратов, обеспечивают получение объективных данных по безопасности, взаимодействию с другими лекарственными средствами в долгосрочной перспективе, а также оценивают соотношения «польза — риск» лекарственных препаратов при практическом применении, — отметил Аудрюс Свейката. — Данные о препарате, которые аккумулируются в рамках стандартной процедуры фармаконадзора, не предоставляют полной информации о возможном развитии нежелательных реакций. Особенность PASS состоит в том, что исследование проводится после регистрации лекарственного препарата. Данные о применении собираются в рутинной медицинской практике, когда врачи не ограничены жесткими рамками, в том числе более строгими критериями отбора, которые сопровождают рандомизированные клинические исследования».

На вопрос модератора о том, когда PASS придут в Россию руководитель Центра по мониторингу эффективного, безопасного и рационального применения лекарственных средств ФГБУ «ИМЦЭУАОСМП» Росздравнадзора Виталий Поливанов ответил, что в настоящее время работа в этой области ведется. Появление нормативных требований, регламентирующих проведение таких исследований, ожидается к 2020 году.

Также было подчеркнуто, что система мониторинга безопасности лекарственных средств в России активно развивается в соответствии с международными требованиями. Профиль безопасности должен отслеживаться на протяжении всего жизненного цикла препарата, в том числе в пострегистрационном периоде. Эти агрегированные данные аккумулируются в отчетах по безопасности препаратов.

Значимость подобных проектов для пациентов и врачей подчеркнул заведующий лабораторией вакцинопрофилактики и иммунотерапии аллергических болезней Научно-исследовательского института вакцин и сывороток им. И. И. Мечникова Михаил Костинов. «Создание грамотно выстроенной практики пострегистрационных исследований в России нужно только приветствовать, — считает эксперт. – Важно только правильно расставить акценты: помнить, что обсуждается не эффективность препарата, а его безопасность; то есть именно то, на что мы должны обращать внимание с момента появления препарата и в течение всего его жизненного цикла. При этом важно оценивать не только клиническую, но и иммунологическую безопасность». По словам эксперта, независимое исследование безопасности иммунобиологических препаратов под государственным контролем должно проводиться регулярно и положительно восприниматься врачебным сообществом.

В заключение, спикеры резюмировали, что первый опыт пострегистрационного международного исследования оригинального российского препарата, инициированного компанией «НПО Петровакс Фарм», повысит интерес к проведению пострегистрационных исследований безопасности другими отечественными компаниями.

Пострегистрационные исследования безопасности (PASS) – это подгруппа пострегистрационных исследований, направленных на изучение и детализацию профиля безопасности лекарственного препарата и/или оценку мер по минимизации рисков медицинского применения.

1 EU PAS Register Guide [EMA/613603/2012]; Guidance for the format and content of the final study report of non-interventional post-authorisation safety studies [EMA/48663/2013]; Guidance for the format and content of the protocol of non-interventional post-authorisation safety studies [EMA/623947/2012]; Guideline on good pharmacovigilance practice (GVP), Module VIII, Rev1 [EMA/813938/2011]

2Регистрационный номер ЕU PAS: ENCEPP/SDPP/12387

Источник публикации: ООО «НПО Петровакс Фарм»

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ccrpsorg · 4 years

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Pharmacovigilance Training

Drug Safety Pharmacovigilance Training

Are you looking to enter clinical research through drug safety jobs? One of the first steps your employers might look for is training. If you have little prior experience in clinical research, you might benefit from certification.

Step One - Becoming a PV

You should always check current entry-level job requirements in drug safety prior to getting training.

Pharmacovigilance Jobs

Estimated Pharmacovigilance Job Salary

Entry Level Pharmacovigilance Job Salary $67,000

Experienced Pharmacovigilance Job Salary $98,000

More than 8-10 Years Experience Pharmacovigilance Job Salary $136,000

Pharmacovigilance (PV) officers collect adverse event data on drugs (Phase 4) to analyse and change warnings for the drug. A minimum of an associate degree is required to take any training course including ours.

Some jobs prefer physicians, nurses, or those with a masters degree in science. The best option for any professional is to get a masters degree in pharmacovigilance, but this is both expensive and takes up to 2 years. A second alternative to landing your first job is by getting drug safety certification.

You can even move up the ladder from simply reporting and collecting adverse effects to being the operations officer. The reality is that large pharma companies need trained officers whose role is to look for and notice issues or side effects of a drug.

Step Two - Benefit of PV Certification

Well, there is a Catch 22. You can’t get a job in pharmacovigilance without experience and you can’t get experience without a job. The

CCRPS pharmacovigilance certification offers online training for research professionals looking to show competency in drug safety monitoring.

Pharmacovigilance jobs are in high demand! You should know that certification or prior experience is needed to get your foot in the door.

We are a nonprofit organization dedicated to providing advanced pharmacovigilance training to students in all tiers of their career.

Our official website offers pharmacovigilance training courses which meet WHO-ISoP and FDA guidelines. The certification modules you complete are based on the most referenced drug safety books.

Like DIA pharmacovigilance training, we provide an online badge that allows employers to verify your certification. We can offer you certification because we are accredited by the ACCRE and main other recognizing accreditors.

Step Three - PV Training Course

Our drug safety and pharmacovigilance training course offers 18 modules:

Online Pharmacovigilance Training Course

3 Monthly Payments of $125 I 2 Monthly Payments of $225 I 1 Payment of $450

Request Scholarship by speaking to our 24/7 chat advisors

1. Pharmacovigilance

2. Basic Definitions used in Pharmacovigilance

3. Medical Dictionary For Regulatory Activities

4. Need for Pharmacovigilance

5. The History of Pharmacovigilance

6. Career Opportunities in Pharmacovigilance

7. Key Skateholders in Clinical Trial Safety

8. Good Communication

9. Pharmacovigilance Methods

10. Information Resources

11. International Organizations and Regulatory Authorities in Pharmacovigilance

12. The Qualified Person for Pharmacovigilance

13. Individual Case Safety Report(s)

14. Signal Detection, Risk Assessment and Management (Pharmacovigilance audit training)

15. Risk Management in Pharmacovigilance

16. Vaccine Pharmacovigilance

17. Setting up of a Pharmacovigilance Centre

18. Post Approval Regulations in Pharmacovigilance

Certification provided at the end of the course.

Step Four - PV Training Center

Pharmacovigilance Training Institute

Our pharmacovigilance training course offers pharmacovigilance certification at reduced scholarship pricing. You can speak with our enrollment advisors to for assistance in pricing and scholarship.

We have trained over 1,800 clinical researchers and are excited to help you take another step towards your journey. Drug safety training can be completed online to show interest when applying to jobs.

This course can be completed in one sitting over a day. After you complete the course, you can instantly update your resume and follow our resources to

Step Five - PV Resources

Some of our favourite resources in pharmacovigilance include:

Getting Started in Pharmacovigilance Part 1

Recruiters Career Pathways in PV

This second section shares a lot of resources on how to apply and get trained in Pharmacovigilance. Note that our course offers certification at a significantly shorter time point and lower price than other courses.

Reading Resources

Cobert’s Manual of Pharmacovigilance and Drug Safety

Mann’s Pharmacovigilance

Drug Safety Data

After being certified in our course; you can apply for entry-level positions in the following roles:

Drug Safety Jobs

Drug safety or Pharmacovigilance scientist (specialist or associate)

Description: The Drug Safety Associate will provide support for Company Operations including SAE reconciliation, ICSR regulatory submissions, generation of SAE listings and data-entry of Individual Case Safety Reports (ICSRs), if required, and support other Pharmacovigilance activities as needed.

Drug safety or PV manager

Description: This position will focus on pharmacovigilance operational aspects to support global pre/post-marketing programs as well as oversight of day-to-day safety activities performed by a Contract Research Organization (CRO).

Safety or PV reviewer

Description: Serve as Medical Scientist with ability to support design, implementation, interpretation, reporting and regulatory filing of clinical studies with a focus and expertise in Patient Safety / Pharmacovigilance (PV). Have responsibility for protecting the patient safety and integrity of clinical studies.

Pharmacovigilance Quality Compliance

Description: The role of the Safety Project Manager is to plan, execute, and finalize projects according to strict deadlines and within budget. Responsibilities include coordination of internal resources to effectively launch Safety Projects, mentor new and existing clients of best practices, and management of study/enterprise accounts. The Safety PM will also define project objectives and oversee quality control through the project life cycle.

Clinical Quality specialist

Description: The Clinical Quality Specialist will be responsible for the coordination of quality metrics across the Enterprise. This position requires daily monitoring of potential core measures candidates to ensure accurate and complete documentation of quality measures; providing education throughout the Enterprise regarding quality measures to all members of the healthcare team; facilitating compliance with all disciplines; and facilitating and participating in problem-solving processes to resolve issues regarding patients, families, physicians, other departments, and staff

Medical Safety scientist/specialist/reviewer

Description: Use principles related to all phases of drug development (pre-clinical through Phase IV) to evaluate clinical data in support of pre & post approval activities; apply pharmacovigilance science, laws, &best practices to interpret data, prepare reports &meet regulatory requirements; appraise methodologies & scientific data/literature on disease states, pharmacology, clinical research & basic science/research to analyze product profile, surveillance and action for risk management; provide technical/medical writing, author scientific publications & communicates data to regulators, researchers and medical community.

Local safety officer

Description:

Prepare and implement health and safety plans for construction projects.

Act as onsite safety representative for the duration of a given contract.

Serve as the SSHO person of contact to conduct the required site and safety analysis and observations.

Evaluate results and make recommendations as necessary for maintaining compliance with regulatory agencies.

Conduct daily safety and health inspections and maintain a written log which includes area/operation inspected, date of inspection, identified hazards, recommended corrective actions, estimated and actual dates of corrections.

Conduct weekly or daily tailgate safety meetings.

Attach safety inspection logs to the contractors’ daily quality control report.

Conduct mishap investigations and complete required reports.

Investigate and resolve health and safety deficiencies.

Must have extensive experience in the field or in a related area.

Must be familiar with standard concepts, practices, and procedures within the environmental and safety compliance fields.

Must be able to accurately establish and keep paper and electronic records concerning equipment, funds, supplies, and other property record information.

Good oral and written communication skills, reading/writing/grammar proficiency, good analytical ability, self-motivated, experienced problem solver, and moderate stress tolerance.

Clinical trial project safety associate (reviewer or specialist)

Description: The Associate Manager, Drug Safety and Pharmacovigilance will report to the Director, Drug Safety and Pharmacovigilance. This individual will be responsible for processing case data, filing of safety related documents, drafting safety narratives based on company templates and meeting safety database standards. This individual will contribute to the successful completion of safety-related goals and objectives in collaboration with the clinical development team. This role requires an individual who is able to perform at a high level in a fast-paced environment. Prior safety-related expertise, with an ability to understand and comply with general pharmaceutical industry rules, regulations, company processes, SOPs and work instructions, particularly in connection with investigational drug safety and pharmacovigilance for clinical studies is essential.

MedDRA coder

Description:

Review and analyze adverse events and determine the appropriate medical MedDRA code

Perform research and retrieve information to address stakeholder inquiries and resolve problems

Provide suggestions and recommendations on improving system- and coding-related procedures

Train other team members in MedDRA coding practices and assist other team members resolve complex issues, provide feedback to help improve quality of project deliverables

Contribute to the development of manuals, guides, SOPs, and presentations

Interface and collaborate with internal and external stakeholders

Pharmacovigilance safety and analytics reporting analyst/specialist/associate

Description:

Initial capture of all event-related information

Review reconciliation reports to identify AE information

Perform the initial triage of AEs including assessment of drug-relatedness and expectedness, coding of the events using MedDRA dictionary and the writing of concise narratives

Conduct follow-up with clinical sites and/or reporting parties to obtain all pertinent adverse event information

Assist with monitoring of compliance (regulatory reporting)

Partner with the Manager Case Management to develop case quality benchmarks and perform regular trending of quality results to identify quality trends or issues. Propose strategies for quality improvement or issue resolution to the Manager, Case Management

Review and contribute to Drug Safety Operations & Drug Safety Quality and Compliance-related SOPs, Work Instructions and job aids particularly where case quality is concerned

Work with Data Management (in-house or vendor) to assure SAE reconciliation between the Clinical Database and Safety Database

Initiate/review processes regarding workflow

Identification and resolution of case processing issues as they arise

Monitoring and problem solving of E2B exchange issues as they arise

Assist with Signal Evaluation and Risk Management (SERM) support, as needed

Assist Clinical Trial support such as safety start-up materials, as needed

Pharmacovigilance Auditor or PV Inspection readiness officer

Description: Regulatory Knowledge - Knowledge of global GVP regulations and guidances; good working knowledge of global GCP, GMP and GLP regulations and guidances. Understands the regulatory environment for global pharmaceutical companies, as well as best practices in the Pharma industry to satisfy regulatory requirements.Industry Knowledge Working knowledge of the pharmaceutical industry and the new drug development process; understands the phases, processes and techniques used in the science of pharmacovigilance.

Safety or Pharmacovigilance Physician (medical director, MD/MBBS, IMG)

Establish/enhance robust surveillance and benefit-risk processes based on clinical and scientific expertise to support Seattle Genetics’ products across the lifecycle

Provide oversight for members of the Safety Evaluation and Risk Management (SERM) group in Global Safety Risk Management

Management of physicians and scientists in the SERM group including recruitment, training, mentoring and development

Establish risk management process starting early in development. Work with clinical teams to develop risk management plans to support Seattle Genetics’ regulatory submissions

Oversee signal management and risk management of Seattle Genetics’ products on a global basis across the life cycle

Work with clinical counterparts as needed, including review clinical study protocols, development plans and serious adverse event handling

Communicate and interact effectively within and across therapeutic teams, and within functional team management as appropriate

Provide pharmacovigilance support for internal and external customers

Provide medical and scientific expertise on pharmacovigilance matters affecting the preparation and submission of timely and accurate information to the regulatory authorities

Work with labeling team to accurately portray the safety profile of assigned drugs or biologics

Provide the training, leadership and continuing education for all departmental staff

Liaise with clinical/medical counterparts across the business to provide PV expertise as needed

Contribute to preparation and review of periodic reports (PADER; PSUR; Annual IND report; 6-monthly line-listings; EU Annual Safety Report; DSUR)

Review and provide medical content, as needed, for key study-related documents, e.g. IB, ICF, SMC/IDMC Charters

Provide input to Pharmacovigilance agreements and interactions

Participate in alliance safety teams with external partner(s)

Participate in protocol development to ensure alignment with risk management plans

Safety Compliance Writer

Description: The ideal candidate will be experienced in Environmental, Safety and Health technical writing with the ability to produce high-quality documentation and/or regulatory requirements that contribute to the overall success of our products. These documents will address compliance and beyond at multiple levels within the client environment.

Other Possible Job Descriptions which qualify under Pharmacovigilance Certification:

Good PV Practices manager

GCP specialist

Pharmacovigilance vendor

Case processing specialist

Clinical trial case processing safety specialist

Post-marketing case processing safety specialist

Epidemiology safety associate (MPH)

Risk management manager

Signal management specialist

Periodic reporting specialist

Regulatory affairs safety specialist

The first step to getting a job in PV or drug safety is the show interest on your resume. Getting certification shows employers that you are interested and dedicated to this field. Enroll in our pharmacovigilance training course to get certified within a day. Payment options include: 3 Monthly Payments of $125, 2 Monthly Payments of $225, and 1 Payment of $450.

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