Attestato di partecipazione
Introduzione
The course will explain the impact of the Clinical Trial Regulation (EU) No 536/2014 on the regulatory and assessment procedures of the safety in clinical trials. Participants will be guided into the regulatory aspects of the major clinical trial application documents and the discussion will cover the rules for safety reporting, tips and tricks for submission of clinical trial application and the substantial modification on the ASR.
The course will address:
- Safety regulatory and assessment procedures under the CTR in a transition period
- Main point to consider related to CTR Q&A document
- Regulatory expectations for a Clinical Trial Application (CTA) submission and modifications during the developmental cycle (Phase I to Phase IV) in safety documents such as Investigator’s Brochure (IB), Reference Safety Information (RSI), protocol
- Regulatory expectations for an Annual Safety Report (ASR) submission
MODULE 1: Safety in clinical trials under the CTR
- Introduction
- Changes of regulatory and assessment procedures under the CTR: Clinical Trial Information System (CTIS)
- Safety reporting in clinical trials
- Breakout sessions and discussion: Hot topic and new challenges related to the CTR
MODULE 2: The Reference Safety Information (RSI)
- Regulatory expectations for a Clinical Trial Application (CTA) submission and modifications during the developmental cycle (Phase I to Phase IV) in safety documents such as Investigator’s Brochure (IB), Reference Safety Information (RSI), protocol
- Focus on the CTR Q&A document: frequent issues and tips and tricks to avoid them
- Breakout sessions, group exercise and discussion: Focus on RSI
MODULE 3: The Annual Safety Report (ASR)
- ASR submission, assessment and regulatory expectations
- ASR writing: format and requirements
- Breakout sessions, group exercise and discussion: How to plan and write your ASR
Professionals involved in the planning, preparation and review of the documents related to clinical trial applications and/or substantial modifications including documents such as Investigator’s Brochures, protocols, Annual Safety Reports, etc.
Professionals who are actively involved in preparation of their organizations to the CTR (EU) No 536/2014 or whose working procedures will be impacted by it.
In particular: Drug Safety and Pharmacovigilance department, Regulatory Affairs department and Quality and Compliance department (e.g. medical writers, pharmacovigilance writers, pharmacovigilance officers, pharmacovigilance managers, QPPVs, safety physicians, managers regulatory affairs and medical evaluators/advisors, document quality and compliance managers).
Participant Experience
Basic knowledge of drug development, safety and/or pharmacovigilance.
Presentation, hands-on exercises using real life anonymized cases, group discussions with a limited number of attendees.
Docente/i
Elena Prokofyeva
Elena Prokofyeva holds a research doctorate from the University of Tuebingen, Germany. She additionally holds a Ph.D. and an M.D. from the Northern State Medical University, Arkhangelsk, Russia, and a Master of Public Health from the University of Umeå, Sweden.
Dr. Prokofyeva joined the FAMHP in 2016 as a drug safety expert. Currently, she is head of drug safety unit at the Department of Research & Development, DG PRE, the FAMHP, Brussels, Belgium. Prior to joining FAMHP she conducted research at Inserm, Paris and worked at a pharmaceutical consulting company in London. Her clinical, research, and industry experience spans a number of topics: drug safety, epidemiology, ophthalmology, cardiovascular and metabolic diseases, health services research, mental diseases, and addictions. She represents Belgium in a safety subgroup of the CTFG. Dr. Prokofyeva initiated and led an update of the Q&A-RSI document within the CTFG which was published in November 2017. She also is actively involved in preparation of CTR Q&A document, and a best practice guide prepared by the CTFG. In addition, she is a part of the working group organized by the European Commission for preparation of an implementing act for the CTR. Dr. Prokofyeva is also part of GCP IWG subgroup in charge of ‘DMC guideline revision’.
This online training is divided in 3 modules:
Module 1 | 26 April 2022 from 09:30 am to 12:30 pm CEST
Module 2 | 28 April 2022 from 09:30 am to 12:30 pm CEST
Module 3 | 03 May 2022 from 09:30 am to 12:30 pm CEST
Some days before the online training you will receive all details about the connection.
The course will proceed with a minimum number of participants. Should this number not be reached the registered participants will be notified one week prior to the commencement of the course.
Early Bird: € 945,00* (until 29 March 2022)
Ordinary: € 1.155,00*
Freelance – Academy – Public Administration**: € 615,00*
* for Italian companies: +22% VAT
** Early Bird discount not applicable to Freelance – Academy – Public Administration fee
The fee includes: tuition, organizational office assistance, teaching materials and attendance certificate that will be sent after the training via e-mail.
Registrati
Versione Stampabile
Cosa saprai fare dopo il corso
Online interactive training on Zoom platform.
LS Academy will provide the access link to the virtual platform a few days before the training.