Check out your Company Bowl for anonymous work chats.
If you haven’t already registered for the UDI and Traceability Forum, do not worry as we got you covered! Quote USDM when registering for the event for 20% off your ticket price http://glassdoor.com/slink.htm?key=vQBXH
Register for our upcoming webinar to gain insight into how medical device manufacturers can benefit from adopting a culture of quality.
FDA's Case for Quality- What You Need to Know
AS USDM expands to EU and UK, USDM Life Sciences Names Holger Braemer, Vice President of EU and UK Division and Managing Director of USDM Europe GmbH in Germany
USDM Life Sciences Names Holger Braemer, Vice President of EU and UK Division and Managing Director of USDM Europe GmbH in Germany
Don't miss tomorrow's live, cutting-edge webinar. The European Parliament just adopted MDR and IVDR. These new regulations mean time is ticking for medical device manufacturers selling devices in the EU to comply. VP of UDI services and solutions, Jay Crowley, will cover a range of related topics to help you prepare. Register now!
New EU Medical Device and Diagnostics (MDR IVDR) Regulations
This Thursday USDM will be hosting a cutting-edge webinar regarding the new EU Medical Device and Diagnostic Regulations (MDR and IVDR). Register now to join VP, Jay Crowley, as he covers a range of topics surrounding the difference between US and EU UDI requirements, solutions, timelines, and more.
New EU Medical Device and Diagnostics (MDR IVDR) Regulations
Pleased to announce that we will be partnering up with the UDI and Traceability Forum, this May in Brussels. We hope that you can join us. To see what we will be discussing with fellow peers and industry supporters, access the brochure here: http://glassdoor.com/slink.htm?key=vQ9YH
UDI 2017 Agenda
Yesterday USDM hosted a Data Health Integrity Webinar which covered: x practical guidance on organizational controls, technical controls and operational factors x optimizing your compliance with data integrity/data reliability principles with a least burdensome approach x how to implement a risk based strategy to audit trail checks If you ever need to gain insight on any of these topics, the webinar can be watched anytime on demand on our website. Check it out!
Data Integrity Health Check
Are you confident in your applied technical controls regarding data integrity? Don't forget to register for tomorrow's live webinar which will be given by USDM's Vice President of Global Regulatory Compliance, Quality Assurance and Auditing. Find out if your life science company is compliant with FDA Data Integrity Guidance.
Data Integrity Health Check
April 5th 2017, The European Parliament approved the In Vitro Diagnostic Medical Devices Regulation and the Medical Devices Regulation. USDM Has been closely following this regulation and is working with medical device companies to help comply. Read the full press release here:
EU Adopts New Diagnostics and Medical Device Regulations, USDM Life Sciences Helps Organizations Comply
USDM and Jay Crowley will be hosting a cutting edge live webinar: "New EU Medical Device and Diagnostics (MDR IVDR) Regulations" to address the timeline, concerns, the differences between US UDI and the IVDR and MDR, Solutions, best practices and more! April 20th. Here is the link for more information:
New EU Medical Device and Diagnostics (MDR IVDR) Regulations