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EU and USA GMP
Inspired Pharma Training
2 พ.ย. 2018
การดู 29,980 ครั้ง
Implementing a QMS - Assigning roles and responsibilities
An Introduction to Good Manufacturing Practice - Pharmaceutical and Biotechnology Industry
Introduction to Analytical Quality by Design (AQbD) principles
The roles of the Heads of Production & QC and the Qualified Person
สาวร้อง ถูกหลอกซื้อบ้านทิพย์ เหยื่อรวมตัวแฉ 'หญิงรุ่นใหญ่' หลอกขายที่คนอื่นให้ สูญกว่า 10 ล้าน
GMP requirements for cell and gene therapy institutions-20201112 0600-1
21 CFR, Parts 210 and 211
Determination of Appropriate GMP's for Excipients
Cleanrooms and Controlled Environments - Trends, Tools, and Technologies
Understanding ICH Q8, 9 and 10
Environmental Monitoring (EM)
Marketing Authorisation in EU| European Medicines Agency (EMA)| MRP, DCP, CP & National Procedure
The Concept of Quality and Quality Definitions
What You Need to Know About the EU GMP Annex 1 Revision
Good Manufacturing Practices for Medicinal Products EU GMP Part 1
GMP 101 - Intro to Good Manufacturing Practice [WEBINAR]
The revised EU & PIC/S GMP Annex 1 - CCN Webinar 2022 10 26
What is Good Manufacturing Practice GMP in Pharmaceuticals?
Revised EU Annex 1- Manufacture of Sterile Products (25 Aug 2022) | Comprehensive Training Module
Cleanroom Training Video