At NPD Consultants, we’re experienced with assisting our clients with the various documents required for clinical evaluation. From CEPs to PMCFs, our consultants help with both the writing and compilation of successful clinical evaluation documentation.
We assist in the writing and updating of various clinical evaluation documents including:
Our team will handle the literature searching for you and conduct a full evaluation of identified clinical data.
We analysis the outputs of your technical documentation before integrating the outputs into the CER.
We ensure your Post-Market Clinical Follow-Ups (PMCFs) and Post-Market Surveillance (PMS) documentation is fully compliant with regulations and organised to a high standard.
Talk with our regulatory consultants for assistance with complying with medical device regulations.