Internal Audit of QMS according to ISO 13485 / UK regulation/ MDSAP / US FDA

At Asphalion we count with Lead Auditors with an extensive track record and experience in the annual review of the QMS suitability and efficiency.

At Asphalion we count with Lead Auditors with an extensive track record and experience in the annual review of the QMS suitability and efficiency.
January 24, 2023

2023 is here and we want to help you! If you are currently planning the audit programme for this year and you are seeking support for the Quality Management System (QMS) internal audit, at Asphalion we count with Lead Auditors with an extensive track record and experience in the annual review of the QMS suitability and efficiency.

It does not matter where you wish to sell your products: Asphalion can perform different types of audits adjusting to the requirements of different regulatory authorities across multiple global markets.

Furthermore, we provide global support in the three main stages of the audit process:

  • Planning: Preparation of audit plan
  • Development: Evaluation of suitability and efficacy of QMS
  • Follow-up: Audit report preparation and CAPA plan definition

 

If you are interested in receiving further details, do not hesitate to contact us at: info@asphalion.com

You can also book a free 30 minutes meeting here: Asphalion Meeting Platform

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