HVAC and GMP Environmental Control - for Pharmaceutical Cleanrooms

Environmental control of pharmaceutical cleanrooms is essential to the manufacture of a quality product. 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. Therefore, the design, validation and ongoing monitoring of a cleanroom HVAC system are necessary to assure the quality and safety of the pharmaceutical product. 

Why Should You Attend:

It is important that a cleanroom’s HVAC system is fully understood, properly designed and properly validated. If this is accomplished, it will provide the environmental control necessary to meet the regulatory particulate and microorganism levels necessary to manufacture quality pharmaceutical product. This webinar will:

Detail and explain the various US and international regulatory requirements for cleanroom classifications.

Who Will Benefit:

This webinar will provide valuable assistance to all personnel in:

Quality Assurance

Environmental Monitoring

Microbiology

Manufacturing

Validation

Engineering

Instructor Profile:

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, Mr Cowan has held various manager / director positions in quality assurance, QC laboratory, technical services validation, manufacturing, and clinical supply manufacturing and distribution. He has taught courses in microbiology at Seneca College (pharmaceutical technology program) in Toronto, Canada.

Note:

Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2016.

For Registration:

http://www.complianceonline.com/hvac-and-gmp-environmental-control-for-pharmaceutical-cleanrooms-webinar-training-703831-prdw?channel=sciencedz