This webinar will discuss the regulations pertaining to objectionable microorganisms, agency expectations, methods to identify objectionable microorganisms, interpreting results, and controls to put into place.
This webinar will review the regulations pertaining to objectionable microorganisms, testing and identifying objectionable microorganisms, and putting appropriate controls into place to prevent harm to the patient. By knowing, where, when, why, and how objectionable microorganisms exist, harmful consequences to the patient can be prevented.
Why Should You Attend:
Objectionable microorganisms are considered, if discovered, harmful to the patient. By identifying and controlling these microorganism and putting the appropriate controls into place early in the pharmaceutical or medical device manufacturing process, problems in the patient can be prevented.This webinar will review the regulations pertaining to objectionable microorganisms, testing and identifying objectionable microorganisms, and putting appropriate controls into place to prevent harm to the patient. By knowing, where, when, why, and how objectionable microorganisms exist, harmful consequences to the patient can be prevented.
Areas Covered in the Webinar:
- Definition of objectionable microorganisms
- Regulations pertaining to objectionable microorganisms
- Identifying objectionable microorganisms
- Tests to determine objectionable microorganisms
- Sources of objectionable microorganisms
- Actions to reduce objectionable microorganism
Who Will Benefit:
- Quality Assurance Managers and Directors
- Quality Control Personnel
- Production Managers
- Microbiology Analysts and Technicians
- Consultants
- Regulatory and Compliance Management
- Regulatory Affairs Professionals
Course Provider
Carl Patterson,
