How To Assemble Your Technical Data To Comply With Medical Device Regulations For Pre-Filled Syringes

Source: West Pharmaceutical Services, Inc.
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Do you have access to all the relevant technical documents to avoid a process delay?

West has created a technical documentation package (TDP) to support your navigation of new document requests. The TDP provides customized information, which helps you easily locate and extract the information needed to support your EU MDR filing process. With direct referencing to Annex I GSPRs, this document will help you minimize the complexity of the entire process.

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