Trainings

Trainings

Training

Next trainings

  • 14 October 2024
  • 19 March 2025
  • Online
Production sites and processes are changing rapidly to adapt to the increasingly stringent requests of regulatory bodies which push towards [...]
Quality & Process
  • 17 October 2024
  • 24 February 2025
  • Online
The training course "Guide to IT infrastructure qualification in GMP environments" aims to delve into the importance of IT infrastructure [...]
Pharma Engineering & Validation
  • 17 October 2024
  • 21 February 2025
  • Online
Investigational Medicinal Products, or IMPs, are defined as "a pharmaceutical form of an active ingredient or placebo that is tested [...]
Quality & Process
  • 18-25 October 2024
  • 7-14 March 2025
  • Online
The training course "The Investigation of Out-of-Specification (OOS) and Out of Trend (OOE/OOT) Analytical Results" aims to provide the tools [...]
Quality & Process
  • 21 October 2024
  • 2 April 2025
  • Online
This training course on Good Distribution Practice (GDP) will explain you the European and local regulatory environment for the distribution [...]
Quality & Process
  • 22 October 2024
  • 17 April 2025
  • Online
The course "Inspections and Audits at the Microbiology QC Laboratory" will examine the most relevant aspects and activities of microbiology [...]
Quality & Process
  • NEW
  • 22 Octobre 2024
  • 26 March 2025
  • Online
Periodic Safety Update Reports, also called PSURs, are pharmacovigilance documents aimed at providing an assessment of the risk-benefit balance of [...]
Pharmacovigilance
  • 22-23 October 2024
  • 25-26 March 2025
  • Online
Have you ever found yourself in the position of not being able to express your feelings effectively or overemphasizing what [...]
Soft Skills
  • 23 October 2024
  • 10 April 2025
  • Online
In the training course “The advertising of medicinal products to healthcare professionals” will approach both general principles of advertising to [...]
Scientific Service
  • 24 October 2024
  • 25 March 2025
  • Online
The training "Focus on the Module 5 of the Common Technical Document (CTD)" starts with an overview of the legal [...]
Regulatory Affairs
  • 4 November 2024
  • 9 April 2025
  • Online

What is auditing in clinical trials and why is it so important? Conducting clinical trials is a complex activity, that [...]

Clinical Research
  • 5 November 2024
  • 8 Apil 2025
  • Online
The Pharmacovigilance System Master File (PSMF) is the key tool for managing the corporate pharmacovigilance system and supporting oversight by [...]
Pharmacovigilance