Join KENX and Compliance Group for hands-on training for engineering, quality, C&Q and validation professionals within the pharmaceutical, biotech, medical device and related industries. Participants can create-their-own-experience by choosing from over 55 tutorials and benefit from the wealth of knowledge and useful material our faculty exchanges. Val-U offers a hands-on experience in which lessons learned turn into immediate, actionable results.
Speakers:
Khaled Moussally
EVP Quality – Clients & Regulatory Relations, Compliance Group
Topic – Understanding the Implications and Opportunities of CSA Draft Guidance on 21 CFR Part 11
Time – 3:30 PM – 4:15 PM on 28th March 2023
Francisco Vicenty
Case for Quality Program Manager, FDA
Topic – Understanding the Implications and Opportunities of CSA Draft Guidance on 21 CFR Part 11
Time – 3:30 PM – 4:15 PM on 28th March 2023
Daniel Walter
Policy Analyst, FDA
Topic – Understanding the Implications and Opportunities of CSA Draft Guidance on 21 CFR Part 11
Time – 3:30 PM – 4:15 PM on 28th March 2023
Stephen Cook
VP – Validation Quality & Compliance, Compliance Group
Topic – Build a Modern Risk-Based CSV Program – An End-to-End Lifecycle Model
Time – 8:45 AM -10:15 AM on 29th March 2023
David Deluca
Engineering Manager – Validation & Data Integrity, Compliance Group
Topic – Qualifying Your Manufacturing Line – Develop a Process Validation Strategy
Time – 1:00 PM -1:40 PM on 29th March 2023
Brianna Novaris
Validation Engineer, Compliance Group
Topic – Qualifying Your Manufacturing Line – Develop a Process Validation Strategy
Time – 1:00 PM -1:40 PM on 29th March 2023
Save $200 on your ticket when you register with code: CG200