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In this webinar you will learn how to identify when sampling plans for other properties are required for things like precision, accuracy, homogeneity and failure rates.
Apr 16, 2018 | 10:00 AM | Monday
How DMFs fit into FDA's regulatory processes for review of drug and biologic applications.
Start on : April 16, 2018 10:00 AM Monday
End on : April 16, 2018 11:00 AM Monday
Why DMFs are important to you and your company , and How DMFs fit into FDA's regulatory processes for review of drug and biologic applications.
Areas Covered in the Session:
Why DMFs are important to you and your company
How DMFs fit into FDA's regulatory processes for review of drug and biologic applications
Why, more than ever, you may need DMFs to maintain current supplier agreements as well as to develop new business relationships
What not to include
Who Will Benefit:
Global Supply Chain
Research and Development
Quality Assurance & Control
Robert J. Russell For the past 9 years, He has been President of RJR Consulting, Inc. The company assists the pharmaceutical, medical device and biotech industries in understanding and complying with International Regulations affecting compliance, new product development, manufacturing and quality assurance.
Event Fee: One Dial-in One Attendee Price: US$150.00
Compliance4All DBA NetZealous,