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6-Hour Virtual Seminar on The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities

November 11 @ 8:00 am - 2:00 pm CST

$545.00

This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together.

Over time, there have been several misunderstandings between supplier / contractors and pharmaceutical / biologic finished product manufacturers. The root of many of the problems lie in a lack of a suitable agreement delineating roles, responsibilities and resolution to agreement to these issues.

Organizer

Global Compliance Panel
Phone:
+1-800-447-9407
Email:
globalcompliancepanel@gmail.com
Website:
http://www.globalcompliancepanel.com

Venue

Online
Compliance Key,364 E Main Street, Suite 1009
Middletown, DE 19709 United States
+ Google Map
Phone:
7172088666
Website:
https://www.compliancekey.us/webinarDetails?industryId=7&webinarid=1596&speakerid=252&source=EI_LN