Speaker Profile
Roger Cowan
Pharmaceutical Consultant, R Cowan Consulting Services LLC
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 37 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.
- 13
- November
- 2024
- Wednesday
Pharmaceutical Compressed Air - Quality GMP Requirements - What you need to know to meet FDA and International Quality Standards
Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product.
Roger Cowan |
Duration:60 Minutes |
Price: ¤150.00
| View Details
- 20
- November
- 2024
- Wednesday
Sterile Filtration of Pharmaceutical Products - What you need to know to meet Validation and Regulatory Requirements
It is important that the sterile filtration process is fully understood and properly validated for your particular application. The process requirements and validation needs differ based on the filtration requirement.
Roger Cowan |
Duration:60 Minutes |
Price: ¤150.00
| View Details
- 27
- November
- 2024
- Wednesday
CMO Supplier Quality Agreements - What you need to know to Comply with New FDA & EU GMP Guidelines for Contract Drug Manufacture
A Quality Agreement is a contract between a pharmaceutical firm and a GMP Contract Manufacturer detailing the responsibilities of each party in assuring the quality, safety, and efficacy of the manufactured drug.
Roger Cowan |
Duration:60 Minutes |
Price: ¤150.00
| View Details
- 4
- December
- 2024
- Wednesday
GMP Environmental Monitoring in Pharmaceutical Clean Rooms
Environmental Monitoring looks at the end results of the Environmental Control program - the microbiological and particulate quality of the clean room.
Roger Cowan |
Duration:60 Minutes |
Price: ¤150.00
| View Details
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. The definition of Environmental Control vs. Environmental Monitoring is discussed. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity and personnel is crucial to protect the product from contamination.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤190.00 | View Details
Pharmaceutical Compressed Air - Quality GMP Requirements - What you need to know to Meet FDA and International Quality Standards
Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product. The design, construction and monitoring of a compressed air system is essential for maintaining a quality system without contamination of the product. Proper testing of compressed air quality according to international standards is important for both validation and ongoing monitoring of the system.
Speaker: Roger Cowan | View Anytime | Price: ¤190.00 | View Details
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. The definition of Environmental Control vs. Environmental Monitoring is discussed. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity and personnel is crucial to protect the product from contamination.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤190.00 | View Details
Pharmaceutical Compressed Air - Quality GMP Requirements - What you need to know to Meet FDA and International Quality Standards
Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product. The design, construction and monitoring of a compressed air system is essential for maintaining a quality system without contamination of the product. Proper testing of compressed air quality according to international standards is important for both validation and ongoing monitoring of the system.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
Sterile Filtration of Pharmaceutical Products -What you need to know to meet Validation and Regulatory Requirements
It is important that the sterile filtration process is fully understood and properly validated for your particular application.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
Sterile Filtration of Pharmaceutical Products -What you need to know to meet Validation and Regulatory Requirements
It is important that the sterile filtration process is fully understood and properly validated for your particular application.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
HVAC and GMP Environmental Control - for Pharmaceutical Cleanrooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤190.00 | View Details
GMP Environmental Monitoring for Pharmaceutical Clean Rooms
Environmental Monitoring looks at the end results of the Environmental Control program - the microbiological and particulate quality of the clean room.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
GMP Environmental Monitoring for Pharmaceutical Clean Rooms
Environmental Monitoring looks at the end results of the Environmental Control program - the microbiological and particulate quality of the clean room.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
HVAC and GMP Environmental Control - for Pharmaceutical Cleanrooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤190.00 | View Details
HVAC and GMP Environmental Control - for Pharmaceutical Cleanrooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤190.00 | View Details
GMP Environmental Monitoring for Pharmaceutical Clean Rooms
Environmental Monitoring looks at the end results of the Environmental Control program - the microbiological and particulate quality of the clean room.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. The definition of Environmental Control vs. Environmental Monitoring is discussed. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity, and personnel is crucial to protect the product from contamination.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤190.00 | View Details
Pharmaceutical Compressed Air - Quality GMP Requirements - What you need to know to meet FDA and International Quality Standards
Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
Sterile Filtration of Pharmaceutical Products - What you need to know to meet Validation and Regulatory Requirements
It is important that the sterile filtration process is fully understood and properly validated for your particular application. The process requirements and validation needs differ based on the filtration requirement.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
CMO Supplier Quality Agreements - What you need to know to comply with new FDA & EU GMP Guidelines for Contract Drug Manufacture
A Quality Agreement is a contract between a pharmaceutical firm and a GMP Contract Manufacturer detailing the responsibilities of each party in assuring the quality, safety, and efficacy of the manufactured drug.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
GMP Environmental Monitoring in Pharmaceutical Clean Rooms
Environmental Monitoring looks at the end results of the Environmental Control program - the microbiological and particulate quality of the clean room.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. The definition of Environmental Control vs. Environmental Monitoring is discussed. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity, and personnel is crucial to protect the product from contamination.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤190.00 | View Details
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. The definition of Environmental Control vs. Environmental Monitoring is discussed. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity, and personnel is crucial to protect the product from contamination.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤190.00 | View Details
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. The definition of Environmental Control vs. Environmental Monitoring is discussed. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity, and personnel is crucial to protect the product from contamination.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤190.00 | View Details
CMO Supplier Quality Agreements - What you need to know to comply with new FDA & EU GMP Guidelines for Contract Drug Manufacture
A Quality Agreement is a contract between a pharmaceutical firm and a GMP Contract Manufacturer detailing the responsibilities of each party in assuring the quality, safety, and efficacy of the manufactured drug.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
Pharmaceutical Compressed Air - Quality GMP Standards and Requirements
Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
Pharmaceutical Compressed Air - Quality GMP Requirements - What you need to know to meet FDA and International Quality Standards
Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
Sterile Filtration of Pharmaceutical Products - What you need to know to meet Validation and Regulatory Requirements
It is important that the sterile filtration process is fully understood and properly validated for your particular application. The process requirements and validation needs differ based on the filtration requirement.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
CMO Supplier Quality Agreements - What you need to know to Comply with New FDA & EU GMP Guidelines for Contract Drug Manufacture
A Quality Agreement is a contract between a pharmaceutical firm and a GMP Contract Manufacturer detailing the responsibilities of each party in assuring the quality, safety, and efficacy of the manufactured drug.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
GMP Environmental Monitoring in Pharmaceutical Clean Rooms
Environmental Monitoring looks at the end results of the Environmental Control program - the microbiological and particulate quality of the clean room.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. The definition of Environmental Control vs. Environmental Monitoring is discussed. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity and personnel is crucial to protect the product from contamination.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤390.00 | View Details
Pharmaceutical Compressed Air - Quality GMP Requirements - What you need to know to Meet FDA and International Quality Standards
Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product. The design, construction and monitoring of a compressed air system is essential for maintaining a quality system without contamination of the product. Proper testing of compressed air quality according to international standards is important for both validation and ongoing monitoring of the system.
Speaker: Roger Cowan | View Anytime | Price: ¤390.00 | View Details
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. The definition of Environmental Control vs. Environmental Monitoring is discussed. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity and personnel is crucial to protect the product from contamination.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤390.00 | View Details
Pharmaceutical Compressed Air - Quality GMP Requirements - What you need to know to Meet FDA and International Quality Standards
Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product. The design, construction and monitoring of a compressed air system is essential for maintaining a quality system without contamination of the product. Proper testing of compressed air quality according to international standards is important for both validation and ongoing monitoring of the system.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
Sterile Filtration of Pharmaceutical Products -What you need to know to meet Validation and Regulatory Requirements
It is important that the sterile filtration process is fully understood and properly validated for your particular application.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
Sterile Filtration of Pharmaceutical Products -What you need to know to meet Validation and Regulatory Requirements
It is important that the sterile filtration process is fully understood and properly validated for your particular application.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
HVAC and GMP Environmental Control - for Pharmaceutical Cleanrooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤390.00 | View Details
GMP Environmental Monitoring for Pharmaceutical Clean Rooms
Environmental Monitoring looks at the end results of the Environmental Control program - the microbiological and particulate quality of the clean room.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
GMP Environmental Monitoring for Pharmaceutical Clean Rooms
Environmental Monitoring looks at the end results of the Environmental Control program - the microbiological and particulate quality of the clean room.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
HVAC and GMP Environmental Control - for Pharmaceutical Cleanrooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤390.00 | View Details
HVAC and GMP Environmental Control - for Pharmaceutical Cleanrooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤390.00 | View Details
GMP Environmental Monitoring for Pharmaceutical Clean Rooms
Environmental Monitoring looks at the end results of the Environmental Control program - the microbiological and particulate quality of the clean room.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. The definition of Environmental Control vs. Environmental Monitoring is discussed. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity, and personnel is crucial to protect the product from contamination.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤390.00 | View Details
Pharmaceutical Compressed Air - Quality GMP Requirements - What you need to know to meet FDA and International Quality Standards
Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
Sterile Filtration of Pharmaceutical Products - What you need to know to meet Validation and Regulatory Requirements
It is important that the sterile filtration process is fully understood and properly validated for your particular application. The process requirements and validation needs differ based on the filtration requirement.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
CMO Supplier Quality Agreements - What you need to know to comply with new FDA & EU GMP Guidelines for Contract Drug Manufacture
A Quality Agreement is a contract between a pharmaceutical firm and a GMP Contract Manufacturer detailing the responsibilities of each party in assuring the quality, safety, and efficacy of the manufactured drug.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
GMP Environmental Monitoring in Pharmaceutical Clean Rooms
Environmental Monitoring looks at the end results of the Environmental Control program - the microbiological and particulate quality of the clean room.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. The definition of Environmental Control vs. Environmental Monitoring is discussed. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity, and personnel is crucial to protect the product from contamination.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤390.00 | View Details
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. The definition of Environmental Control vs. Environmental Monitoring is discussed. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity, and personnel is crucial to protect the product from contamination.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤390.00 | View Details
HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. The definition of Environmental Control vs. Environmental Monitoring is discussed. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity, and personnel is crucial to protect the product from contamination.
Speaker: Roger Cowan | View Anytime | Duration: 75 Minutes | Price: ¤390.00 | View Details
CMO Supplier Quality Agreements - What you need to know to comply with new FDA & EU GMP Guidelines for Contract Drug Manufacture
A Quality Agreement is a contract between a pharmaceutical firm and a GMP Contract Manufacturer detailing the responsibilities of each party in assuring the quality, safety, and efficacy of the manufactured drug.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
Pharmaceutical Compressed Air - Quality GMP Standards and Requirements
Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
Pharmaceutical Compressed Air - Quality GMP Requirements - What you need to know to meet FDA and International Quality Standards
Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
Sterile Filtration of Pharmaceutical Products - What you need to know to meet Validation and Regulatory Requirements
It is important that the sterile filtration process is fully understood and properly validated for your particular application. The process requirements and validation needs differ based on the filtration requirement.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
CMO Supplier Quality Agreements - What you need to know to Comply with New FDA & EU GMP Guidelines for Contract Drug Manufacture
A Quality Agreement is a contract between a pharmaceutical firm and a GMP Contract Manufacturer detailing the responsibilities of each party in assuring the quality, safety, and efficacy of the manufactured drug.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details
GMP Environmental Monitoring in Pharmaceutical Clean Rooms
Environmental Monitoring looks at the end results of the Environmental Control program - the microbiological and particulate quality of the clean room.
Speaker: Roger Cowan | View Anytime | Duration: 60 Minutes | Price: ¤390.00 | View Details