Before acquiring a product or portfolio, it is important to ascertain that there are no outstanding development and regulatory issues, especially in a highly regulated field. Regulatory due diligence will help to decide on the acquisition, based on potential regulatory compliance risks.
DDR’s expertise covers many therapeutic areas (dermatology, neurology, etc.) and different types of products: Drugs, Medical Devices and Cosmetics.
DDR will anticipate and identify pending regulatory obligations, ensuring that all information is accurate and reflects current scientific and regulatory requirements.
How can DDR help?
- DDR offers a complete regulatory accompaniment supporting the consortium activities during the whole project’s development, thanks to our gained experience and several successes in multi-national collaboration proposals granted by the EC.
- DDR will contribute to the preparation of proposals from early stages.