Apr 16, 2018 | 10:00 AM | Monday

Mon Apr 16, 10:00 AM - Mon Apr 16, 11:00 AM
in 2 days
616 Corporate Way STE 2-5332, New York, NY 10989

Community: Upper West Side

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Description

How DMFs fit into FDA's regulatory processes for review of drug and biologic applications.

Event Details

Overview:
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:
Manufacturing
Regulatory Affairs
Project Managers
Global Supply Chain
Research and Development
Quality Assurance & Control

Speaker Profile:
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

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
Understanding and Meeting your Regulatory & Processing Responsibilities

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