Speaker Profile


Roger Cowan

Pharmaceutical Consultant, R Cowan Consulting Services LLC

Roger Cowan is the founder and owner of R Cowan Consulting Services LLC. Roger has more than 30 years of direct experience in pharmaceutical quality assurance and manufacturing at major pharmaceutical companies in Canada and the U.S. In his career, Roger has held various manager/director positions in Quality Assurance, QC Laboratory, Technical Services Validation, Manufacturing, and Clinical Supply manufacturing and distribution. His experience covers management of the Clinical Supplies Manufacturing Facility and handling GMP and ISO audits from both domestic and international regulatory agencies. He has extensive experience in GMP audits covering various suppliers and contract manufacturing organizations.

Roger's areas of expertise include aseptic pharmaceutical manufacture, GMP facility audits, technical transfer, microbiology, environmental monitoring/contamination control, product sterilization, process development, process validation, clinical supply manufacturing, labeling and distribution, US / International regulatory requirements, regulatory submissions, and quality assurance/control.

CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacturers
CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacturers

Speaker:Roger Cowan
Time: 24th January 2019 10:00 AM PDT | 01:00 PM EDT
Duration:60 Minutes
Model : PMAQ-9128

Thu
24
Jan 2019

GMP Environmental Monitoring for Pharmaceutical Clean Rooms
GMP Environmental Monitoring for Pharmaceutical Clean Rooms

Speaker:Roger Cowan
Time: 10th January 2019 10:00 AM PDT | 01:00 PM EDT
Duration:60 Minutes
Model : PMAQ-9126

Thu
10
Jan 2019

Pharmaceutical Compressed Air - Quality GMP Standards and Requirements
Pharmaceutical Compressed Air - Quality GMP Standards and Requirements

Speaker:Roger Cowan
Time: 4th June 2019 10:00 AM PDT | 01:00 PM EDT
Duration:60 Minutes
Model : PMAQ-9127

Tue
04
Jun 2019

Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements
Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements

Speaker:Roger Cowan
Time: 27th June 2019 10:00 AM PDT | 01:00 PM EDT
Duration:60 Minutes
Model : PMAQ-9269

Thu
27
Jun 2019

No recorded webinars to list here.
No cd/dvd's available.