Event : Quality Agreements with Pharmaceutical - Biologic Manufacturers and the Use of Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities - Webinar By GlobalCompliancePanel http://www.rsc.org/events/detail/6736/Quality%20Agreements%20with%20Pharmaceutical%20-%20Biologic%20Manufacturers%20and%20the%20Use%20of%20Drug%20Master%20Files%3a%20Understanding%20and%20Meeting%20your%20Regulatory%20and%20Processing%20Responsibilities%20-%20Webinar%20By%20GlobalCompliancePanel This is a feed for event : Quality Agreements with Pharmaceutical - Biologic Manufacturers and the Use of Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities - Webinar By GlobalCompliancePanel Thu, 11 Sep 2014 13:13:13 +0100 6736 6736 http://www.rsc.org/events/detail/6736/Quality%20Agreements%20with%20Pharmaceutical%20-%20Biologic%20Manufacturers%20and%20the%20Use%20of%20Drug%20Master%20Files%3a%20Understanding%20and%20Meeting%20your%20Regulatory%20and%20Processing%20Responsibilities%20-%20Webinar%20By%20GlobalCompliancePanel Quality Agreements with Pharmaceutical - Biologic Manufacturers and the Use of Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities - Webinar By GlobalCompliancePanel Event dates: 8 December 2011<br/>Event summary: This combined Quality Agreement and DMF (Drug Master Files) training will discuss the advantages for suppliers and drug product manufacturers developing these arrangements together.<br/>Event Venue: online training, Wilmington, 19801, United States Thu, 11 Sep 2014 13:13:13 +0100 2014-09-11T13:13:13+01:00