I3CGLOBAL REGHELPS PVT LTD Press Releases - EIN Presswire

Published on December 11, 2025 - 18:16 GMT

IVDR CE Certification: Low Manufacturer Awareness as Self-Declared Devices Now Require Notified Body Oversight

IVDD Self-Declared Devices Now Require Notified Body Assessment Under IVDR NEW DELHI, INDIA, December 11, 2025 /⁨EINPresswire.com⁩/ -- I3CGLOBAL, a leading global regulatory compliance consulting organization, has issued an urgent industry advisory …

Distribution channels: Companies, Emergency Services ...

Published on October 21, 2025 - 04:35 GMT

IVDR Consultancy Expanded Globally by I3CGLOBAL for In Vitro Diagnostic Manufacturers

IVDR Consultancy by I3CGLOBAL expands to help global IVD manufacturers achieve CE Marking compliance under EU IVDR 2017/746 efficiently. NEW DELHI, DELHI, INDIA, October 21, 2025 /⁨EINPresswire.com⁩/ -- I3CGLOBAL, a global leader in medical device and in …

Distribution channels: Chemical Industry, Healthcare & Pharmaceuticals Industry ...

Published on October 13, 2025 - 00:00 GMT

I3CGlobal and Reghelps SRC Collaborate to Deliver Comprehensive IVD Performance Evaluation Services for CE Marking

The partnership combines I3CGlobal's regulatory expertise with Reghelps SRC CRO’s capabilities to streamline IVD Performance Evaluation and CE certification. BANGALORE, KARNATAKA, INDIA, October 13, 2025 /⁨EINPresswire.com⁩/ -- I3CGLOBAL, a leading …

Distribution channels: Business & Economy, Chemical Industry ...

Published on April 29, 2025 - 06:30 GMT

ISO 13485 Certification – I3CGLOBAL Launches New Strategies for Early Audit Success

Introduces early stage audit readiness solutions to streamline ISO 13485 certification for medical device and IVD companies inline with MDR, IVDR and FDA QMSR CHARLOTTE, NC, UNITED STATES, April 29, 2025 /⁨EINPresswire.com⁩/ -- I3CGLOBAL, a global leader …

Distribution channels: Business & Economy, Healthcare & Pharmaceuticals Industry ...

Published on April 7, 2025 - 04:05 GMT

I3CGlobal Unveils Regulatory Driven Cybersecurity Strategy for Software Medical Devices

The core concept of FDA 510k software medical device clearances BANGALORE, KARNATAKA, INDIA, April 7, 2025 /⁨EINPresswire.com⁩/ -- The integration of software into medical devices has revolutionised healthcare by enabling real-time patient monitoring, …

Distribution channels: Business & Economy, Emergency Services ...

Published on March 14, 2025 - 08:20 GMT

I3CGLOBAL expands WHO Prequalification (WHO PQ) consulting services for Global IVD manufacturers

The new service streamlines technical documentation and QMS under one roof BANGALORE, INDIA, March 14, 2025 /⁨EINPresswire.com⁩/ -- I3CGLOBAL, a leading medical device and Invitro diagnostic regulatory consulting firm has enhanced its WHO Prequalification …

Distribution channels: Business & Economy, Healthcare & Pharmaceuticals Industry ...

Published on March 14, 2025 - 07:20 GMT

USFDA inspection on the rise over Indian Medtech industry

BANGALORE, INDIA, March 14, 2025 /⁨EINPresswire.com⁩/ -- Indian pharmaceutical, nutraceutical, and medical device manufacturers are making significant progress in strengthening Good Manufacturing Practice (GMP) compliance, positioning the country as a …

Distribution channels: Food & Beverage Industry, Healthcare & Pharmaceuticals Industry ...