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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online, 10777 Westheimer Suite 1100, Houston, 77042, United Kingdom

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Organised by

compliance2go

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compliance2go
10777 Westheimer Suite 1100, Houston, 77042, United States of America
18777824696
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