A well performed due diligence process is challenging but crucial in any merger and acquisition (M&A) decision or investment planning. It is fundamental for the acquiring party to get a sound assessment of the quality, regulatory and clinical evidence situation to understand any potential risks and vulnerabilities. The medical device regulatory landscape is complex and changing.
Strengthening the due diligence team with a QAdvis Medical Device quality/regulatory expert or clinical expert will significantly increase the chances of a successful project. Our team is working according to a defined and well proven due diligence model that is adapted to each project. Each project is unique and deserves its individual setup.
A due diligence is different from compliance audits and the team members use all experience to prioritize and select review–segments correctly along the investigation process within the time budget.
You can trust our confidential, professional, and respectful engagement.