EU Medical Device Regulation PMO and Project Delivery

Regardless of your internal resources, it could be extremely taxing and unrealistic to expect your team to accomplish both their normal daily activities as well as the work necessary to ensure compliance with the new set of requirements per the EU Medical Device Regulation (MDR). Although both are critical to the success of your medical device, the strain of handling all aspects of EU MDR transition internally can cause avoidable mistakes and unnecessary delays in getting your product to market.

Find out how ProPharma Group can provide your medical device team with the project management support needed to ensure your product is compliant with all aspects of EU MDR requirements.

Case Study



The Cost of Poor Project Management

Project Management isn’t for the faint of heart. There is a shockingly high rate of project failure… but on the other hand, great project management can be a key differentiator that leads a company...


Free Webinar: Effective FDA Engagement

FDA faces challenges (like new technology) and new review models (like real world evidence) that stretch agency standards and practices. At the same time, imperatives like product safety and efficacy...


Successfully Passing MHRA Inspections for Overseas Manufacturing Sites

ProPharma Group offers GMP and GDP compliance services from clinical development to commercial distribution of the products' lifecycle. ProPharma Group’s Compliance and Quality team completed the...