Five certifications, every one of them earned.
The regulatory and quality marks that cover the work we do. None of them is a sticker on a brochure; each one is an active process we maintain for every install.
- CDSCO
Central Drugs Standard Control Organisation
All medical devices we supply and import are registered with CDSCO. We handle the registration transfer as part of the install scope.
- AERB
Atomic Energy Regulatory Board
For every CT and PET install, we handle the AERB layout approval and the commissioning certificate.
- ISO 13485
ISO 13485 — Medical devices quality management
Our refurbishment process is documented against ISO 13485, the international standard for medical-device quality management systems.
- NABL
National Accreditation Board for Testing and Calibration Laboratories
Our service team works to NABL-traceable calibration standards for all calibrated equipment.
- MSME
MSME Registered
Registered under the Micro, Small and Medium Enterprises Development Act. UDYAM registration on file.
How the paperwork is handled
CDSCO and AERB paperwork is part of the project, not an extra. We file everything; you sign three documents (the CDSCO declaration of end-use, the AERB layout undertaking, and the post-installation radiation safety undertaking).
For a typical MRI install, the full CDSCO + AERB trail adds 3-4 weeks to the project timeline, scheduled in parallel with civil work.
Ask the team that handles the paperwork.
A short note about the project and the location. We'll reply with the specific regulatory trail and a written timeline.