DURHAM, N.C., February 26, 2019 — The European Union’s new Medical Device Regulation will mean a lot of changes for device makers when it takes effect in May 2020. Now’s the time to prepare, and Premier Research will discuss how at a live webinar on Tuesday, March 12.
Topics will include:
- When device makers need to be compliant with the MDR
- How the rules will affect development of new products — and those already on the market
- Why the changes make it essential to have a well-developed regulatory strategy
Register today to attend The EU’s New MDR Compliance Rules: Your Questions Answered. The hour-long webinar starts at 11am EDT / 3pm GMT / 4pm CST.
About Premier Research
Premier Research, a midsize clinical research company, is dedicated to helping biotech, specialty pharma, and device innovators transform life-changing ideas and breakthrough science into new medical treatments.
As a global company, Premier specializes in the use of innovative technologies for smart study design and trial management to deliver clean, conclusive data to sponsors. Whether it’s developing product lifecycle strategies, reducing clinical development cycle times, securing access to patients, navigating global regulations, maximizing the impact of limited rare disease data, or providing expertise in specific therapeutic areas, Premier is committed to helping its customers answer the unmet needs of patients across a broad range of medical conditions.