Trainings

Trainings

Training

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  • 15 January 2025
  • Online

In the pharmaceutical industry, especially in sterile production, environmental monitoring (EM) of classified areas and utilities plays a fundamental role [...]

Quality & Process
  • NEW
  • 30 Gennaio 2025
  • Online
Da ottobre 2015 è in vigore l’Annex 15 delle GMP Europee. Con questa revisione anche aspetti di processo moderno sono [...]
Quality & Process
  • 18 & 19 February 2025
  • Online

During the training course "Medical Device Regulatory Affairs", key issues for those who want to operate or work in this [...]

Medical Device
  • 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
  • 21 e 28 February 2025
  • Online
Il corso di formazione “Studi di Stabilità nello Sviluppo Farmaceutico e nella Produzione” si propone di illustrare i criteri secondo [...]
Quality & Process
  • 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
  • 25-26 February2025
  • Online

Il Corso Trainer the Trainer offre un programma formativo mirato alle aziende che desiderano sviluppare
competenze interne per la [...]

Soft Skills
  • NEW
  • 27 February 2025
  • Online
The training course "Regulatory affairs of dietary supplements and novel foods" has the primary objective of delving into the industry [...]
Food Supplements
  • 28 February 2025
  • Online

Il 31 gennaio 2022 è entrato in vigore il Regolamento UE 536/2014 (CTR) andando ad abrogare la Direttiva 2001/20/CE (CTD).<br [...]

Clinical Research
  • NEW
  • 4 March 2025
  • Online
Smoke studies are critically important tests that visualize air flows within contamination-controlled environments. Airflows can be vehicles of contamination and [...]
Pharma Engineering & Validation
  • 5 March 2025
  • Online
Medical and scientific literature is a valuable source of information on medicinal products. Marketing authorization holders (MAHs) are required to [...]
Pharmacovigilance
  • 5-6 March 2025
  • Online
What is a Pharmacovigilance Quality System and why is it important? According to current regulations, it is the responsibility of [...]
Pharmacovigilance