A practical guide to IDMP preparations
Essential next steps to maximise the benefits of a data-driven future
IDMP is an unprecedented opportunity to transform regulatory product data management and unlock new efficiencies. In this whitepaper we present the next steps for aligning technology, process, operating models, change activities, and data strategies to maximize benefits.
Iperion life sciences consultancy becomes part of Deloitte
Our commitment to promote data standardisation for better patient outcomes
Life Sciences Consultancy will become a Deloitte business. Combining our forces to make a greater contribution to the accelerated approval of new or improved medicines as well as the provision of high-quality information to patients and the healthcare sector.
European Medical Device Regulation
The complexity of qualification and classification
The European Medical Device Regulation 2017/745 (EU-MDR) provides a regulatory framework with the purpose of ensuring safe and effective performance of medical devices before and after these are brought to the EU market.