At NPD Consultants, we help our clients with successful technical documentation submissions. We lend an experienced hand to both the writing and compiling of these documents to ensure they help you achieve the desired results for your medical devices.
We fully organise and structure your technical documentations for UK MDR and EU MDR submissions.
Our consultants are experts in design control, and we work with you to create a design and development process that suits your requirements.
Our team can write all the required technical documents for you including:
We will do all the liaising for you, speaking with other technical experts and integrating external documents on your behalf.
Talk with our regulatory consultants for assistance with complying with medical device regulations.