Post Market Surveillance

[ISO 13485 Cl 8.2.1]

Post Market Surveillance

Conduct the PMS of the medical devices, post release into the market. Applicable to the devices placed in European Union.

INTERNAL AUDIT TOOL

1. IMPORTANT INFORMATION - Step 1 of 6

Certainly, we will be happy to provide you with a detailed service proposal for European Authorized Representative and allied services. To do so, please provide us with the following information:

Manufacturer Name *

Address *

Address Line 1

Address Line 2

City

State / Province / Region

Postal Code

Country

Website / URL

ISO 13485 PRICING

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ISO 13485 PROPOSAL REQUEST

Frequently Asked Questions

Should a manufacturer maintain single procedure for purchasing and outsourcing ?

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How to control an Outsourcing vendor? How to maintain documents

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