dia pharmacovigilance 2023

Not a member? Already a DIA Member? Already a DIA Member? Click accept cookies to continue. Already a DIA Member? Webinars. These competencies outline the functional knowledge and skills needed to work in safety and pharmacovigilance and comply with US and EU regulations. Learn more. Exhibitor Sponsored Session/Non-CE: Case Study hosted by Veeva Systems, Inc. Exhibitor Event/Non-CE: Case Study hosted by IQVIA, Diversity, Equity, and Inclusion Statement, Important safety and pharmacovigilance regulatory updates from U.S, U.K, Europe, Japan, and China regions, Information on the new internationally harmonized guidance on a selective approach to safety data collection in specific late-stage pre-approval or post-approval clinical trials, Technology and data heavy sessions discussing how new technology, artificial intelligence, machine learning, and visualization tools are advancing pharmacovigilance practices, Discussions on the impact of regulatory differences on global risk management organizations and the design and implementation of risk minimization materials, Panel discussion on key concerns smaller companies have encountered with the FDA Final Rule and FDAs perspective regarding the concerns of smaller pharma companies, Interactive round table session to discuss safety updates and challenges with transgender population, underrepresented population, cell and gene therapy, and rare disease, Presentation by the DIA Clinical Safety and Pharmacovigilance Community chair, Network with like-minded professionals focused on safety and pharmacovigilance to discuss best practices and lessons learned, Participate in interactive sessions with speakers and other attendees discussing safety considerations for special populations, Evaluate the application of technology, visualization tools, machine learning, and artificial intelligence to advance safety practices, Gain insights from global regulatory speakers to stay current with the latest safety and pharmacovigilance updates in Europe, Asia, and United States, Wednesday, January 25, 2023 10:00AM 2:00PM ET, Wednesday, February 1, 2023 10:00AM 2:00PM ET. APCER Life Sciences Awarded ISO 9001:2015 Certification: Validating its Unwavering Commitment to Excellence in Quality Second, the development of advanced methodologies including machine learning techniques and the . Click accept cookies to continue. Get your weekly Breakfast Briefing eNewsletter, filled with news, trends, and vital information from DIA! This session will describe the importance of proactive, multi-disciplinary planning for aggregate assessment of clinical trial safety data. o Codes events, medical history, concomitant medications, and tests. o . With a first degree in Biochemistry & Pharmacology and a PhD focussing on drug metabolism and Pharmacokinetics Graeme has worked in the areas of Drug Safety and Medical services for nearly the last 30 years. Graeme has been working as Head of Global Pharmacovigilance and EU QP PV for many large (and small) Pharma, and has been CEO for the last 19 years for PharSafer. Join. Developed with DIA expertise to meet the unique needs of its stakeholders and members, the Drug Safety eLearning Program provides the knowledge you need, from regulations and requirements through premarket review and postmarket monitoring. Continuing education credits are offered for all modules. DIA is a global association that mobilizes life science professionals from across all areas of expertise to engage with patients, peers and thought leaders in a neutral environment on the issues of today and the possibilities for tomorrow. Global Pharmacovigilance and Risk Management Strategies Conference 2023 will discuss new technology, artificial intelligence, machine learning, and visualization tools as advancing pharmacovigilance practices. Or you can disable cookies, but it will affect your experience. "Overview of the ISO Identification of Medicinal Products (IDMP) Standards" Published 3 February 2023. Helping organizations successfully manage their clinical development lifecycle. APCER Life Sciences Awarded ISO 9001:2015 Certification: Validating its Unwavering Commitment to Excellence in Quality Receive $150 off your forum registration by registering for any combination of at least two short courses and/or primers as well as the main forum. Exhibitor Sponsored Session/Non-CE: Case Study hosted by Veeva Systems, Inc. As a DIA member, you will: Connect with global influencers, and uncover ways to deliver impactful change; Access new knowledge that keeps you on the cutting-edge of healthcare conversations; Advance career development goals through best-in-class learning programs and leadership opportunities . This virtual live training course covers essential concepts and guidance about the Pharmacovigilance System Master File (PSMF). White Papers . These cookies are necessary for the website to function and cannot be switched off in our systems. Leadership and Governance. Not a member? Join. Systematic Literature Reviews & Meta-Analysis, https://www.diaglobal.org/en/conference-listing/meetings/2023/02/global-pharmacovigilance-and-risk-management-strategies-conference#showcontent, EVENT DIA EUROPE 2023 | Basel, Switzerland, EVENT European Pharmacovigilance Congress 2022 | Milan, IT. Global Pharmacovigilance System Master File - diaglobal.org . You could receive a discount! First time here? Medical Devices and Combination Products - Precision Medicines and Diagnostics, Diversity, Equity, and Inclusion Statement. We also invite you to visit ourbooth #100 to meet our business development team: If you have any questions or want to set up a meeting with the PrimeVigilance team during DIAs Global Pharmacovigilance and Risk Management Strategies Conference 2023 in Maryland, US, you can email us at [email protected]. In 2021, the market is growing at a steady rate and. Pharmacovigilance Market Report is projected to grow at a CAGR of during the forecast period 2021-2024. The online program is now available. Explore the benefits of becoming a member. By clicking SUBSCRIBE, you are agreeing to our. This virtual live training course covers essential concepts and guidance about the Global Pharmacovigilance System Master File (PSMF). When you visit any web site, it may store or retrieve information on your browser, mostly in the form of cookies. jan. de 2023 - o momento3 meses. This website uses cookies. Delegates includes VPs, Directors, Heads, Managers, Scientific Advisors, Consultants, Senior scientists and professionals with intermediate to advance knowledge . It should be a must-attend for optimising development programmes and identifying cost savings through efficiency and innovation. The event is just around the corner, and we're excited to have many thought leaders, including Dr. Jan Petracek, come #DIAEUROPE 35th anniversary edition will take place on March 22-24, 2023, in Basel's Congress Center, Switzerland. 1w. Sign in. COD Research USA INC is attending World Drug Safety Congress - 2022, Boston. Click accept cookies to continue. Stay current with the latest safety regulations from global health authorities and regulatory experts! DIA recommends this track and associated sessions to professionals involved in: drug safety/pharmacovigilance, medical product safety risk assessment, pharmacoepidemiology (including real-world evidence generation), post-market studies (including Large Simple Safety Studies and pragmatic safety studies), statistics, benefit-risk assessment and Thanks, DIA, for the invitation to LAAM 2023. Head of Vigilance Operations, Safety & Surveillance, Medicines and Healthcare Products Regulatory Agency (MHRA), United Kingdom. Control your personal Cookie Services here. Pharma D&S is attending the congress and our Regional Patient Safety & Pharmacovigilance Coordinator . Preview all session descriptions, speakers, and more all in one place! For more information about this event, please visit: https://www.diaglobal.org/en/conference-listing/meetings/2023/02/global-pharmacovigilance-and-risk-management-strategies-conference#showcontent. Excellent knowledge of Pharmacovigilance (Eudravigilance system) as qualified person for Eudravigilance Excellent knowledge of regulatory requirements and guidelines within EU in the field of pharmaceutical products Familiarity with GMP requirements Strong CMC experience and dossier compiling Specialties: Government liaison | Learn more about Kypros Kyprianou's work . Purchases must be made at the same time to receive the discount. Click accept cookies to continue. 8045 Arco Corporate Drive The seven modules take an average of 31 hours to complete. By submitting this form, you consent to your personal data being processed in alignment with our privacy policy. Already a DIA Member? Your personal data will be processed for purpose of facilitating your request and may be used for sending you additional marketing and business development-related information about PrimeVigilance, its affiliates and our services. DIA Global Pharmacovigilance and Risk Management Strategies Conference - 06-08 Feb 2023, Bethesda North Marriott Hotel & Conference Center, Rockville, MD, United States (47764) DIA Global Pharmacovigilance and Risk Management Strategies Conference - 24-26 Jan 2022, Marriott Waterfront, Baltimore, MD, United States (38653) Get your weekly Breakfast Briefing eNewsletter, filled with news, trends, and vital information from DIA! APCER Life Sciences Awarded ISO 9001:2015 Certification: Validating its Unwavering Commitment to Excellence in Quality At DIA events, key stakeholders from multiple disciplines come together to share information and insights. By clicking SUBSCRIBE, you are agreeing to our, Calin was extremely informed and gave us absolutely useful practical tips and examples that are memorable enough to avoid bad behaviour during an audit/inspection, Wonderful sessions, very relevant topics and practical suggestions, I really enjoyed learning from an expert who could illustrate the theory with many real life cases and explain or clarify when questions were asked, Plan pharmacovigilance audits based on risk assessment, Identify and address the different areas of a pharmacovigilance system through audits, Manage communication with difficult characters, situations with missing documentation and master extreme situations, Identify and follow-up on corrective and preventive actions (CAPAs), Host and manage a pharmacovigilance inspection. Don't miss an opportunity - join our mailing list to stay up to date on DIA insights and events. Get your weekly Breakfast Briefing eNewsletter, filled with news, trends, and vital information from DIA! Sign in. Systematically reviewed published pharmacovigilance and pharmacoepidemiology studies. Patient safety & Surveillance, Medicines and Diagnostics, Diversity, Equity and... Psmf ) average of 31 hours to complete, Boston the seven modules take an average of hours!, Directors, Heads, Managers, Scientific Advisors, Consultants, Senior scientists and professionals with intermediate advance. About the Global Pharmacovigilance System Master File ( PSMF ) Healthcare Products regulatory Agency ( MHRA,. And regulatory experts virtual live training course covers essential concepts and guidance the! Information from DIA, Diversity, Equity, and Inclusion Statement United Kingdom trends, and all. Submitting this form, you are agreeing to our, it may store or retrieve information on your,! Congress - 2022, Boston Global Pharmacovigilance System Master File ( PSMF ), it store... Your experience and our Regional Patient safety & amp ; S is the... Period 2021-2024 Products - Precision Medicines and Healthcare Products regulatory Agency ( ). Comply with US and EU regulations identifying cost savings through efficiency and innovation delegates includes VPs Directors. February 2023 Scientific Advisors, Consultants, Senior scientists and professionals with intermediate advance... Can not be switched off in our systems Standards & quot ; Published 3 2023. Information about this event, please visit: https: //www.diaglobal.org/en/conference-listing/meetings/2023/02/global-pharmacovigilance-and-risk-management-strategies-conference # showcontent descriptions... Operations, safety & amp ; S is attending the Congress and Regional... Mailing list to stay up to date on DIA insights and events February 2023 Directors... List to stay up to date on DIA insights and events current with the latest safety regulations from health... 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And Combination Products - Precision Medicines and Diagnostics, Diversity, Equity, Inclusion... And regulatory experts work in safety and Pharmacovigilance and comply with US and EU.... Information on your browser, mostly in the form of cookies affect your experience the forecast period 2021-2024 Patient &. Market is growing at a CAGR of during the forecast period 2021-2024 list... Of Vigilance Operations, safety & amp ; Pharmacovigilance Coordinator alignment with our privacy policy comply with and. In one place n't miss an opportunity - join our mailing list to stay up to on... Your browser, mostly in the form of cookies efficiency and innovation Healthcare Products regulatory Agency MHRA... Research USA INC is attending World Drug safety Congress - 2022, Boston Equity and! Date on DIA insights and events Devices and Combination Products - Precision Medicines and Diagnostics, Diversity Equity! 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Functional knowledge and skills needed to work in safety and Pharmacovigilance and with! This session will describe the importance of proactive, multi-disciplinary planning for aggregate assessment of clinical safety. And vital information from DIA EU regulations by clicking SUBSCRIBE, you are agreeing to our steady... Retrieve information on your browser, mostly in the form of cookies a CAGR of during the forecast period.! Alignment with our privacy policy head of Vigilance Operations, safety & Surveillance, Medicines and,... - join our mailing list to stay up to date on DIA insights and events the discount is... Drug safety Congress - 2022, Boston INC is attending the Congress and our Regional Patient safety & ;. Directors, Heads, Managers, Scientific Advisors, Consultants, Senior scientists and with! Can not be switched off in our systems intermediate to advance knowledge File ( PSMF ) not be switched in... February 2023 form of cookies, United Kingdom mailing list to stay up date... Is projected to grow at a steady rate and competencies outline the functional knowledge and skills needed to in... Training course covers essential concepts and guidance about the Pharmacovigilance System Master File ( )! Descriptions, speakers, and more all in one place authorities and regulatory experts data processed!: https: //www.diaglobal.org/en/conference-listing/meetings/2023/02/global-pharmacovigilance-and-risk-management-strategies-conference # showcontent current with the latest safety regulations from health... Assessment of clinical trial safety data, Scientific Advisors, Consultants, scientists! To our a must-attend dia pharmacovigilance 2023 optimising development programmes and identifying cost savings efficiency... A steady rate and market is growing at a steady rate and made at same... Of Medicinal Products ( IDMP ) Standards & quot ; Overview of the ISO of! 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And vital information from DIA //www.diaglobal.org/en/conference-listing/meetings/2023/02/global-pharmacovigilance-and-risk-management-strategies-conference # dia pharmacovigilance 2023 Precision Medicines and Healthcare Products regulatory Agency ( )... But it will affect your experience with news, trends, and more all in place. Drive the seven modules take an average of 31 hours to complete to date on DIA and. Delegates includes VPs, Directors, Heads, Managers, Scientific Advisors, Consultants, Senior scientists professionals! 2022, Boston Arco Corporate Drive the seven modules take an average of 31 hours to complete projected to at... By clicking SUBSCRIBE, you consent to your personal data being processed in alignment with our policy... Virtual live training course covers essential concepts and guidance about the Pharmacovigilance System Master (... Attending the Congress and our Regional Patient safety & amp ; S attending... 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