Online
Showing 33–48 of 48 results
-
Sale!
Validering av analysmetoder
€ 1,230 Add to cart -
An overview of IEC 62304 Medical Device software
€ 0 Add to cart -
Applying Control Charts for Visualizing and Detecting Trends
Read more -
Decontamination Process and the new Draft of the EU GMP Annex 1
Read more -
EN ISO14971:2019 – Risk management – in relation to MDR and ISO13485
Read more -
Equipment Management in the Pharmaceutical Supply Chain
Read more -
GMP Update series – What’s cookin’ – October 2020
Read more -
How to Qualify your Suppliers in Compliance with GMP
Read more -
Introduction à la réglementation sur les Dispositifs Médicaux
Read more -
IVDR Readiness – prepare for the changes in the new IVDR
Read more -
Maintaining Temperature Compliance for Pharmaceuticals in the Supply Chain
Read more -
New perspectives on Cross Contamination and Cleaning validation
Read more -
Post Market Clinical Follow-Up for a Medical Device
€ 0 Add to cart -
Sale!
Regulatory Affairs Manager – Medical Devices
€ 620 Add to cart -
Remote audits – Why, when and how
Read more -
Starting materials – the GMP essentials
Read more
