Our regulatory and quality management experts will review your standard operating procedures (SOPs) to make sure they comply to the new Medical Device Regulation (EU) 2017/745 (MDR) and any related standards or regulation. As SOPs often involve multiple people and departments it can be helpful to bring in a fresh pair of eyes to review all requirements from start to finish. This service will analyse every aspect of an SOP in relation to the MDR, wider regulation and the standards you require – spanning departments, standards, drafts and documents that can include Good Clinical Practices (ISO GCP), Risk Management (ISO 14971), Post-Market Surveillance (PMS), Quality Management Systems (QMS, ISO 13485, MDSAP), and Unique Device Identifier (UDI), and more.
To request a quote please use the contact form to send us:
Your contact details
The number of documents and pages you would like checked.
The regulation(s) and standard(s) your SOP(s) should be checked against (e.g. ISO 13485:2016).