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.
January 24, 2023
At Asphalion we count with Lead Auditors with an extensive track record and experience in the annual review of the QMS suitability and efficiency.
We are happy and proud to welcome Adi Ickowicz as Senior Principal to further strengthen our Medical
Scientific advice is about advising medicine developers on the most appropriate way to generate robust evidence on
📆 13-14 October, 2022 💻 Online course ASPHALION expert André Mota, together with other
Watch Asphalion Regulatory expert, Mireia Roig as she reviews the UK regulatory landscape and goes through what
What is the Access Consortium? The consortium is a medium-sized coalition of regulatory authorities from Australia, Canada,
Asphalion offers Regulatory solutions in the UK and support with MHRA requirements: Strategy and operational support Pre-approval
📆 20st September, 2022 🕕3:00- 4:00 p.m. CEST With Brexit behind us and the UK establishing
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