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MDD & IVD Directive’s move away and New medical device regulations in Europe will be released this year.

Countdown begins for launch of the new ISO 13485:2016 standard!!!

US FDA Food Contact Material restrictions. What and How to get approved

Pre-Clinical Investigation & Evaluation for Medical Device

Message from Our desk

New 2014 EU Commission Requirements Impacting CE Certification Lead Times by European Notified Bodies

I 3 CONSULTING announces the launch of new product QARA

Today, LIBERTY MANAGEMENT GROUP, USA announces the Business Association with I 3 CONSULTING, INDIA.