I 3 CONSULTING announces the launch of new product QARA
[CLOUD based documentation for U.S.A and European Medical Device, Drugs, Cosmetic & Food Regulatory compliance]
8th Sep 2014
I 3 CONSULTING today announced the worldwide release of the QARA the world’s first of its kind, exclusive very convenient cloud based regulatory compliance documentation system for Medical Device CE Marking, ISO 13485, 21 CFR 820 & FDA 510k. It also supports US FDA Drug Master File preparation.
The biggest advantage for the client is to have complete control on files and get moment to moment update about the work.
Criteria to avail the service
Language of communication ENGLISH
No matter where the consultant or client. No worry about consultant travel and allied expenses.
The QARA pricing is very much affordable to all small scale medical device manufacturers (OEM) and own brand labelers (OBL).
The price details can be checked in www.i-3-c.com.
About I 3 CONSULTING
I 3 CONSULTING, a company formed by a group of professionals in the year 2000 from Pharma, Microbiology, Biotechnology, Engineering with a vision to capture the small scale manufacturers regulatory compliance business. The company in association with Liberty Management Group (LMG) and MedDeviceCorp (MDC) has successfully served more than 3500 clients so far from all over the world. The company focuses on Medical Device CE Marking (CE Certification) with European Notified Bodies. The team working with us are practically qualified to handle any type and class of device.
Mr. Sunil Francis
Head of Customer Relations