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2018 - What you need to know to Meet FDA and International Quality Standards

Date2018-10-12

Deadline2018-10-11

VenueFremont, USA - United States USA - United States

KeywordsManufacturing; Microbiology; Engineering

Websitehttps://www.compliance4all.com/control/w...t_2018_SEO

Topics/Call fo Papers

Overview:
This webinar will take you through the primary sources of compressed air
contamination. It will also detail GMP standards and requirements
pertaining to compressed air quality.
Why should you Attend:
Compressed air is often overlooked as a potential source of clean room
and product contamination. This webinar will give you an understanding
of the different types of contamination inherent in compressed air and
how to prevent each from affecting your particular system.
Areas Covered in the Session:
Compressed Air - Importance of Quality
Pharmaceutical Compressed Air System Design
Contamination Types and Sources
Contamination Prevention
International GMP Testing Standards
Testing Methods and Specifications
Who Will Benefit: This webinar will provide valuable assistance to all
personnel in Pharmaceutical Manufacturing and Compounding Pharmacies:
Quality Assurance
Environmental Monitoring
Microbiology
Manufacturing
Validation
Engineering
Maintenance
Speaker 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 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.
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support-AT-compliance4All.com

Last modified: 2018-08-10 14:33:09