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Labquality can help medical device manufacturers in creating a regulatory plan.
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When planning on bringing a medical device to the market, a company needs to create a regulatory plan to define the regulatory framework (including standards and guidance) The conformity assessment procedure determines the actions and documentation needed for the regulatory submission of the device as well as the requirements Conformity assessment procedures are set out in Article 52 and Annexes IX to XI of MDR (2017/745), and in Article 48 and Annexes IX to XI of IVDR (2017/746). The applicable conformity assessment procedure depends on the type and risk class of the device, both of which need to be defined in the regulatory plan. |
✔ Labquality’s experts can help your company in creating a regulatory plan.
✔ When creating regulatory plans for medical device manufacturers, we consider and include all the required and necessary aspects to find the most feasible approach to the regulatory submission.
WE ALSO OFFER TRAINING ON THE SUBJECT:
Efficient introduction – Regulatory Essentials in Health Tech – training series >>