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.
Batch Production Record and Device History Record Review and Quality Assessment
13 August 2014, Houston, United Kingdom
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online, 10777 Westheimer Suite 1100, Houston, 77042, United Kingdom
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compliance2go
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compliance2go
10777 Westheimer Suite 1100, Houston, 77042, United States of America
1.877.782.4696
Contact us by email
10777 Westheimer Suite 1100, Houston, 77042, United States of America
1.877.782.4696
Contact us by email
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