There are a number of ways Peritus Regulatory can help from a due diligence perspective:
Evaluation of proposed development & registration of therapeutics / Medical devices
Regulatory analysis of product portfolios i.e., for venture capital firms
Identification of potential regulatory matters for licensing in or out
Advising on applicable guidelines for regulatory dossiers
Advice on registration strategy and health authority requirements
Independent evaluation of adherence to regulations including evaluation of the technical data, data from nonclinical & clinical phases, manufacturing and CMC
Please contact us for support and questions in any regulatory matter related to products and medical devices.