Introduction

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.

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Venue

Online

Online, 10777 Westheimer Suite 1100, Houston, Texas, USA, 77042, Houston, 77042, United States

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Organised by

compliance2go

Contact information

compliance2go
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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