Events 2018 - 30.3.2018 - One Day Training Course, Free for BADI members
Topics: Cosmetic products - update, Food supplements - update; Foodvigilance and market surveillance; Metabolic syndrome - prevention in men and women; Medicines with well-established use; GDPR Directive; Bioprinting, 3D and 4D printing in medicinal products;
Registration | Lecturers | Sessions | Coffee Break
- 01.06.2018 - Annual Conference
Topics: Regulatory Update - Brexit, Market Access (HTA); Off-Label Use of Medication for Children; Orphan Drugs; Drug Supply - Falsified Medicinal Products – update
Registration | Lecturers | Sessions | Coffee Break
- 26 - 28.09.2018 - Intensive f2f Training course
Topic: Foundation Skills in Medical Information 2018 - Introduction to Regulatory Affairs, Preclinic, Clinical Trials, Medical Information and Market Access (HTA)
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- 09.11.2018 - eCTD One Day f2f Training Course
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- 19.10.2018 - Module 1, Drug Drug Regulatory Affairs Training Course`18
Topics: Market Access (HTA) in the different MSs (France, Sweden, Germany) and reimbursement decisions;
Falsified Medicinal Products - update;
New Medical Device Regulations: Regulation (EU) 2017/745; Regulation (EU) 2017/746;
Drug Shortages; EU parallel trade - Shortages (framework challenges in Bulgaria);
Good distribution practice (GDP) - overview and challenges;
Regulatory update: Brexit Implications for the MAHs (innovative and generics) - follow up, part II;
Registration | Lecturers | Sessions | Coffee Break
- 02.11.2018 - Module 2, Drug Drug Regulatory Affairs Training Course`18
Topics: Pharmacovigilance Part I: PRAC activities, New Developments and important recommendations in PV-Referrals - Critics and possible approaches; PASS experiences; Experiences with the implementation of the EudraVigilance System launched on 22 November 2017, for centrally reporting and monitoring of suspected adverse reactions;
European PHv-Law, The EU-Pharmacovigilance System, PSMF, QPPV, Assessment of Pharmacovigilance Information; Access Policy; Signal Detections, PHV-Inspections. Activities with Educational materials in Germany: “Blue Hand”;
Roles and responsibilities of Sponsor/MAH and safety service provider;
Registration | Lecturers | Sessions | Coffee Break
- 23.11.2018 - Module 3, Drug Drug Regulatory Affairs Training Course`18
Topics: Pharmacovigilance Part II: Functionality of EVDAS; PSMF; MLM;
Vaccine Safety;
Registration Process in Eudravigilance Data Base and responsibilities of sponsor and their representatives;
Be more successful at quality checks with analysis of audit questions;
Cannabis for medicinal use - regulatory perspective, applicatons in medicine, legal framework.
Registration | Lecturers | Sessions | Coffee Break
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