Complete Range of Testing Services as per the Compulsory Registration Scheme Including Phase V
Every telecom equipment must undergo mandatory testing and certification prior to sale, import of use in India.
In Vitro Diagnostic Medical Device Regulation (IVDR)
TÜV Rheinland LGA Products GmbH is a EU designated Notified Body under the In Vitro Diagnostic Device Regulation (IVDR 2017/746).
Medical Device Centre of Excellence
TÜV Rheinland’s world-class facility in AMTZ, Vizag offers testing of medical and non-medical devices for Biomaterial, EMI/EMC, Reliability, Acoustics & Electrical Safety Testing.