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 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.
Related Resources
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...
Successfully Passing MHRA Inspections for Overseas Manufacturing Sites
ProPharma offers GMP and GDP compliance services from clinical development to commercial distribution of the products' lifecycle. ProPharma’s Compliance and Quality team completed the first on-site...
Navigating the Generic Drug Application and Approval Process
Navigating the generic drug application and approval process can be challenging. From pre-filing through post-approval, find out exactly what needs to be done for your Abbreviated New Drug...