If you missed R&Q's Paul Robinson discuss UDI during R&Q's afternoon workshop at BIOMEDevice in April, here's a second chance. A similar presentation and discussion will be offered in conjunction with MassMEDIC on Wednesday, May 18th at 11:30am EST. All the details - including the link to register - are below!
What?
A Whole New World of UDI: How To Seamlessly Comply with the FDA Now While Preparing for the Global Requirements of the Future
Surprisingly, about 50% of medical device companies have not yet started implementing the requirements for UDI compliance. Have you? And if you have, what are you plans regarding the expanding UDI global requirements? With some deadlines in the rearview mirror and others rapidly approaching, standing still is not an option. Using real-world experiences, this webinar will offer strategic advice for complying with UDI in the US and around the world, including compliance dates, detailed task planning, and other specific needs you’ll need to meet – and perhaps most importantly, pitfalls to avoid. Whether you are ahead of the UDI game or have waited until the eleventh hour, this webinar will offer a combination of basic and advanced information that anyone dealing with UDI cannot pass up. Be compliant, and be on time.
Who?
Host: MassMEDIC
Speaker: Paul Robinson, Senior Director of Regional Operations,
Regulatory and Quality Solutions (R&Q)
When?
Wednesday, May 18th
11:30am - 12:30pm EST