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

Sterile Filtration of Pharmaceutical Products - 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

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

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

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

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

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

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

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

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