Typical Elements Required to be Included in the Batch Production Record and the Device History Record in order to Accomplish a Quality and Cost Effective Review and Quality Assessment based on current Regulatory Expectations.
Live Webinar-Batch Production Record and Device History Record Review and Quality Assessment
13 August 2014, Houston, United States
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Online, 10777 Westheimer Suite 1100, Houston, Texas, USA, 77042, Houston, 77042, United States
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compliance2go
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compliance2go
10777 Westheimer Suite 1100, Houston, Texas, USA, 77042, Houston, 77042, United States of America
(877) 782-4696
Contact us by email
10777 Westheimer Suite 1100, Houston, Texas, USA, 77042, Houston, 77042, United States of America
(877) 782-4696
Contact us by email
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