Compliance & Product Regulatory ApproVals

Relaxation for Class C & D Medical Devices

CDSCO has recently released a notification dated 12th Oct regarding the importing class C & D medical devices. As per the notification, the existing importers or manufacturers importing the class C & D medical devices can import the devices without MD-15 licenses for next 6 months from the date of notification provided condition that application of the devices have been submitted as per medical device rule 2017.  

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Praveen Rao

CEO & Technical Director, C-PRAV Group: Australia, New Zealand, India & Canada 

C-PRAV Labs & Certifications 

Professional engineering experience of 30+ years with technical and managerial skills obtained from professional degree, courses, and hands-on experience, while working with organizations and companies involved in Design & Development, Testing, Inspection, Certification and Compliance (TICC). 

Management of electrical/electronic products & systems Testing and Certifications for Global markets in Consumer, Industrial, IT, Telecom, Defence, Medical, and Automotive Industries. Overall advisory for Standards, Regulations, Testing and Certifications for Global Market Access (GMA). 

  • ISO/IEC 17025 Lab Quality Management 
  • NATA Authorised Signatory (1995 to 2000) for EMC Testing 
  • NATA & IANZ Authorised Technical Assessor (current)
  • EMI/EMC, RF/Wireless, EMR-RF Exposure/SAR 
  • NATA Technical Assessors Advisory Committee (current) 
  • Current Chair of Australian EMC National Standards Committee 
  • Member of Australian National standards committees for Safety, Radio, RF Exp/SAR 
  • Represent Australia in International Standards committees like IEC, CISPR, IEEE 
  • Member of Telecommunications Certification Body Council, USA and European REDCA