28 Oct 2014, New Jersey – Freyr announces the launch of its FREYR UDI VISION – a three part webinar series that will provide an in-depth view and explain the intricacies and nuances of UDI submission process based on the real-time case scenarios, queries and challenges faced by medical device companies.
The series will comprehensively cover UDI Class I, II and III compliance mandates, challenges, and roadmap along with demonstrations by UDI experts on how to prepare and achieve UDI compliance in a simplified manner.
SESSION 1 – UDI READINESS: Friday, 14th Nov, 2014
SESSION 2 – UDI LABELING & BARCODING: Friday, 21st Nov, 2014
SESSION 3 – DI and PI: Friday, 5th Dec, 2014
The webinar series is a must for all for regulatory executives from medical device companies who are looking to get a thorough understanding about successfully implementing UDI for their products.
To learn more details about the webinars, speaker panel and registration are available at
Headquartered in New Jersey, USA, with Global Operations and Delivery Centers in UK, Middle East, South Africa, and AsiaPac, Freyr is a specialized full service Global Regulatory Solutions and Services Company, exclusively focusing on the entire Regulatory value-chain of Life Sciences companies.
Freyr offers Consulting, Software & Operational Services of Regulatory Affairs, Operations & Information Management functions to Large & Small-Medium Life Sciences companies in a highly cost-effective model.
Freyr’s rapidly growing team of 350+ regulatory and technology professionals possess real-time global solution expertise to provide diverse services across the regulatory landscape. Freyr’s Global Operations, Delivery and Development Centers are ISO 9001:2008 & ISO 27001:2013 certified.
For more information please visit www.freyrsolutions.com
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