SEMINARS & RECORDED WEBINAR COURSES

Seminars

Recorded Seminars

Recorded Webinars

COURSES

 

Reclassification of Software Automated Medical Devices

 

Data Integrity in GMP and GCP: Compliance with FDA, EMA, and MHRA Requirements

 

The US FDA QMSR Transition - 21 CFR 820 and ISO 13485

 

Writing SOP’s and Work Instructions that Really Work

 

Practical Implementation of Pharmaceutical Quality Risk Management (QRM)

 

IQ, OQ, PQ in the Verification and Validation Process

 

How to Reduce Human Error in a GMP Manufacturing Floor

 

The Key Elements of Being “Recall-Ready”: What FDA Expects When Time Is Critical

 

The CSA Playbook for SaaS, PaaS & Modern Digital Platforms - 3-Hour Course

 

Technical Writing Excellence in the Life Sciences - A Masterclass