Purchase any WEBINAR and get
Validity : 25th Sep'23 to 05th Oct'23
Quality and Supply Chain Oversight for Virtual Companies – what is different and what are the Challenges?
Specific Quality System Aspects for Virtual Companies
Batch Certification – Minimum Requirements & Best Practices
Use of Quality Risk Management
Post Product Release Oversight Responsibilities
Participants in this seminar will:
You should attend the webinar to learn how to:
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation; including, process/product validation, facilities validation, 21 CFR Part 11, test method validation, equipment/automated processes and cleaning validation.