Live Online Training/Webinars - Regulatory Affairs

Drug Master File Procedures in the EU, the US and Japan - Live Online Training

6/7 September 2022

Drug Master File Procedures in the EU, the US and Japan - Live Online Training Taking into account the guidance on metal impurities (ICH Q3D) and genotoxic impurities (ICH M7)

China GMP and Registration for APIs - Live Online Training

Tuesday, 4 October 2022 13.00 - 16.30 h

China GMP and Registration for APIs - Live Online Training

GMP for Herbal Medicinal Products (HMPs) + Post Conference on Qualification & Validation Aspects for Cannabis - Live Online Conference

8/9 November 2022

GMP for Herbal Medicinal Products (HMPs) + Post Conference on Qualification & Validation Aspects for Cannabis - Live Online Conference

GMP for Herbal Medicinal Products (HMPs) - Live Online Conference

8/9 November 2022

GMP for Herbal Medicinal Products (HMPs) - Live Online Conference

ICH Q12 Training Course - Live Online Training

15/16 November 2022

ICH Q12 Training Course - Live Online Training How to use the PACMP in Practice

Setting Specifications and Acceptance Criteria - Live Online Training

6/7 December 2022

Setting Specifications and Acceptance Criteria - Live Online Training

GMP meets Regulatory Affairs - Live Online Training

7/8 February 2023

GMP meets Regulatory Affairs - Live Online Training Applying for and maintaining marketing authorisations: What you need to know from a GMP perspective

API Regulatory Starting Materials - Live Online Training

9/10 February 2023

API Regulatory Starting Materials - Live Online Training

How to register APIs in Brazil - Live Online Training

Tuesday, 28 February 2023 10.30 - 16.00 h

How to register APIs in Brazil - Live Online Training

Global Registration and Life Cycle Management of APIs - Live Online Training

28-30 March 2023

Global Registration and Life Cycle Management of APIs - Live Online Training Contents of the regulatory information in the ASMF and CEP

Live Online Training/Webinars by Topics