2019 - Current Regulatory Requirements for Sterile Products
Date2019-08-13
Deadline2019-08-13
VenueOnline Event, USA - United States
Keywords21 CFR 210-211; 21 CFR part 820; Laboratory control
Topics/Call fo Papers
Review the current regulatory requirements and guidance documents dealing with sterile products
Review the expectations for aseptically produced products.
Discuss the six quality systems that are reviewed during regulatory inspections
Review common deficiencies cited with the manufacture of sterile drugs
Review the importance of personnel training and control of microbiological contamination
Review the expectations for aseptically produced products.
Discuss the six quality systems that are reviewed during regulatory inspections
Review common deficiencies cited with the manufacture of sterile drugs
Review the importance of personnel training and control of microbiological contamination
Other CFPs
- Orphan Drug Development History & Overview
- Patient Access of Medical Records under HIPAA - HHS Guidance and Compliance Objectives
- Teaching your Front-line How to Ask BSA Questions?
- Live Webinar Effective Social Media Use in HR
- Live Webinar Transforming HR through Six Sigma: Adopting a New Way of Thinking About Human Resources
Last modified: 2019-07-02 04:42:22