Trainings

Trainings

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Category

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  • 22 May 2024
  • Online
In the pharmaceutical industry, especially in sterile production, environmental monitoring (EM) of classified areas and utilities plays a fundamental role [...]
Quality & Process
NEW
  • 23 May 2024
  • Online
The training course “Engineering guidelines in the pharmaceutical” is intended to address in a practical manner the engineering methods and [...]
Pharma Engineering & Validation
  • 23 May 2024
  • Online
This training course on Good Distribution Practice (GDP) will explain you the European and local regulatory environment for the distribution [...]
Quality & Process
  • 23-24 May 2024
  • Online
The training course “Drug-device combination products in EU and US” will explore the EU and US regulatory landscape defining the [...]
Medical Device
  • 24 May 2024
  • Online
The Pharmacovigilance System Master File (PSMF) is the key tool for managing the corporate pharmacovigilance system and supporting oversight by [...]
Pharmacovigilance
  • 24 May 2024
  • Online
Analytical validation, according to the criteria described in the ICH Q2 guideline, has been applied in the pharmaceutical industry for [...]
Quality & Process
  • 27-28 May 2024
  • Online
The training course "Statistical tools for pharmaceutical quality control" wish to provide useful tools for understanding and making the best [...]
Quality & Process
  • 29 May 2024
  • Online
The training course "Guide to IT infrastructure qualification in GMP environments" aims to delve into the importance of IT infrastructure [...]
Pharma Engineering & Validation
  • 30-31 May 2024
  • Online
Recently, some of the most common critical findings in regulatory pharmacovigilance inspections are being given for signal detection and management, [...]
Pharmacovigilance
  • 30 May 2024
  • Online
The training course "Regulatory affairs of dietary supplements and novel foods" has the primary objective of delving into the industry [...]
Food Supplements
  • 3 June 2024
  • Online
The training "Focus on the Module 5 of the Common Technical Document (CTD)" starts with an overview of the legal [...]
Regulatory Affairs
  • June 4th 2024
  • Online
The training course "APR, PQR and CAPA System" is structured in two parts: the first will explain the current regulatory [...]
Quality & Process