


Executive Conference Corporation
The mission of ECC Webinars is to provide the pharmaceutical, biotech, and medical device industries with leading edge and informative webinars led by experts in their fields, fostering a stronger knowledge base in the workforce.
"The Difference is Distictive"
Instructor
Roger Cowan
Roger Cowan is the founder and owner of R Cowan Consulting Services LLC, a consulting company specializing primarily in the area of pharmaceutical contract manufacturing. He has 35 years experience in pharmaceutical quality assurance and manufacturing. 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. Roger has taught courses in microbiology at Seneca College (Pharmaceutical Technology Program) in Toronto, Canada.
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.
Roger Cowan: Upcoming and Archived Webinars
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ECC-736
04/07/2026
upcoming
GMP Environmental Monitoring for Pharmaceutical Clean Rooms
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ECC-729
03/03/2026
archive
CMO Supplier Quality Agreements – How to Comply with new FDA and EU Guidelines for Contract Drug Manufacture
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ECC-722
02/03/2026
archive
Pharmaceutical Compressed Air - Quality GMP Standards and Requirements
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ECC-716
01/20/2026
archive
Sterile Filtration of Pharmaceutical Products – Validation and Regulatory Requirements
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ECC-714
12/11/2025
archive
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
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ECC-709
11/13/2025
archive
Sterile Filtration of Pharmaceutical Products – Validation and Regulatory Requirements
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ECC-707
10/23/2025
archive
GMP Environmental Monitoring for Pharmaceutical Clean Rooms
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ECC-706
09/04/2025
archive
Pharmaceutical Compressed Air - Quality GMP Standards and Requirements
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ECC-677
08/14/2025
archive
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
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ECC-680
08/06/2025
archive
CMO Supplier Quality Agreements – How to Comply with new FDA and EU Guidelines for Contract Drug Manufacture
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ECC-676
06/11/2025
archive
Sterile Filtration of Pharmaceutical Products – Validation and Regulatory Requirements
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ECC-655
05/01/2025
archive
Pharmaceutical Compressed Air - Quality GMP Standards and Requirements
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ECC-672
04/30/2025
archive
GMP Environmental Monitoring for Pharmaceutical Clean Rooms
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ECC-666
04/09/2025
archive
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
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ECC-664
03/26/2025
archive
Sterile Filtration of Pharmaceutical Products – Validation and Regulatory Requirements
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ECC-663
03/20/2025
archive
CMO Supplier Quality Agreements – How to Comply with new FDA and EU Guidelines for Contract Drug Manufacture
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ECC-657
12/11/2024
archive
GMP Environmental Monitoring for Pharmaceutical Clean Rooms
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ECC-650
11/12/2024
archive
GMP Environmental Monitoring for Pharmaceutical Clean Rooms
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ECC-644
10/08/2024
archive
HVAC and GMP Environmental Control – for Pharmaceutical Clean Rooms
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ECC-632
09/04/2024
archive
Pharmaceutical Compressed Air – Quality GMP Standards and Requirements
