"We provide knowledge and information about CGMP and Quality Systems to the Life Science industry"

GMP and Quality systems training - Webinars

Webinars that features hot topics in an efficient and timely way.

It's a very flexible and effective course concept.
You save time, travel expences and spare the environment.

Previously public webinars that are still current are available for purchase as recordings.

Public webinars - Calendar

2020

3.6

Corrective Action Planning – Keys to Success   #5815 (Pharma and Medical Device)

15.6

GMP responsibilities for MAH – new draft from EMA   #5809 (Pharma)

16.6

Decontamination Process and the new Draft of the EU GMP Annex 1   #5818 (Pharma)

18.6

New perspectives on Cross Contamination and Cleaning validation   #5819 (Pharma)

22.6

Equipment Management in the Pharmaceutical Supply Chain; with a Focus on Calibration   #5820 (Pharma)

1.9

Acceptance Sampling Plans: Inspection by Attributes   #5821  (Medical Device)

9.10

Acceptance Sampling Plans: Inspection by Variables   #5822  (Medical Device)

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Recorded webinars

The following webinars are sold as recordings:

Audits
» MDR Audit Readiness – prepare for your MDR certification Audit 
» Remote audits - Why, when and how  
 
Combination products
» Updates on Combo Products – Final FDA Guidance published!
 
Medical Device regulations
» Get to know the new Medical Device and IVD Regulations - Prepare for the transition
» EN ISO14971:2019 - Risk management
- understand its importance and relation to MDR and ISO13485

Pharmaceuticals
» GMP responsibilities for MAH – new draft from EMA
» New EU GMP Annex 1 draft 2020 – learn about it now!

Distribution of pharmaceuticals (GDP)
» Maintaining Temperature Compliance for Pharmaceuticals in the Supply Chain

Statistics: Test Method Validation / Process Validation (Medical Device)
» Keeping Score – Measuring Process Capability
» Valid Statistical Techniques Made Easy - Test Method Validation, Part 1
» Valid Statistical Techniques Made Easy - Test Method Validation, Part 2
» Sampling: How Much Is Enough for Process Validation?
» Statistical Techniques for Process Validation Made Easy - Part 1
» Statistical Techniques for Process Validation Made Easy - Part 2
» Keeping Score – Measuring Process Capability
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