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BIS CRS Registration for Wireless Speakers — IS 616 India 2026

Complete 2026 guide to BIS CRS Registration for Wireless and Bluetooth Speakers under IS 616 in India. Covers who must register, documents, the 6-step process, mandatory tests, penalties, and expert support from Rego Services Pvt. Ltd.

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BIS CRS Registration for LED LCD Smart TV 32 Inches and Above India 2026 — IS 616 Complete Guide

Complete 2026 guide to BIS CRS registration for Plasma, LED, LCD, and Smart TVs with screen size 32 inches and above under IS 616:2010/IS 616:2017.

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bis crs registration laptop notebook tablet india 2026

BIS CRS Registration for Laptops, Notebooks & Tablets in India 2026

IS 13252 (Part 1):2010 explained, the Authorised Indian Representative requirement, and the 8-step BIS registration process.

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bis crs registration electronic video games india 2026

BIS CRS Registration for Electronic Video Games | Rego Services

Ensure compliance with mandatory BIS CRS Registration for electronic video games, gaming consoles, and handheld gaming devices in India. Learn about IS 616 requirements, product testing, documentation, BIS certification procedures, and regulatory obligations for manufacturers and importers seeking market access in 2026.

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bis crs registration amplifiers 2000w above india 2026

BIS CRS Registration for Amplifiers with Input Power 2000W and Above — IS 616 India 2026 | Rego Services

Complete 2026 guide to BIS CRS Registration for Amplifiers with Input Power 2000W and Above under IS 616 India — mandatory tests, documents, 6-step process, and expert support from Rego Services.

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bis crs registration ups inverter india 2026

BIS CRS Registration for UPS and Inverters India 2026

Complete 2026 guide to BIS CRS registration for UPS and Inverters under IS 16242 (Part 1):2014 (≤5 KVA) and IS 16242 (Part 1):2025 (≤10 KVA).

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Smartwatch BIS registration compliance guide

BIS CRS Registration for Smart Watches in India 2026 — Complete Guide | Rego Services

Complete 2026 guide to BIS CRS registration for Smart Watches under IS 13252 (Part 1). Covers WPC approval, document checklist, the step-by-step process, and how Rego Services helps manufacturers and importers.

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BIS CRS certification for storage batteries

BIS CRS Registration for Storage Batteries in India 2026 | Rego Services

Complete 2026 guide to BIS CRS registration for Storage Batteries under IS 16270:2014. Covers why registration is mandatory, the 4 certification components, document checklist, the 6-step process for domestic and foreign manufacturers, and how Rego Services helps importers.

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BIS certification for lithium-ion batteries

BIS CRS Registration for Lithium-Ion Batteries India 2026 | Rego Services

Complete 2026 guide to BIS CRS registration for Lithium-Ion Batteries under IS 16046:2018 — 10 mandatory tests, document checklist, 7-step process, and expert support from Rego Services.

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BIS CRS Registration for Electronic & IT Products India

Complete 2026 guide to BIS CRS Registration for electronic and IT products in India — eligible products, required documents, 5-step process, penalties, and expert support from Rego Services.

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BIS parallel testing for electronics certification

BIS Parallel Testing for Electronics & IT Goods India 2026 | Rego Services

Complete 2026 guide to BIS Parallel Testing under CRS — how it saves 4–13 weeks, eligible products, 6-step process, limitations, and expert support from Rego Services.

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BIS CRS registration for polyphosphoric acid

BIS CRS Registration for Polyphosphoric Acid in India 2026

IS 17439:2020 explained, the document checklist, and the 7-step BIS registration process for manufacturers and importers.

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BIS Registration Certificate for Importers in India 2026: Complete Compliance Guide

Get a BIS Registration Certificate to import products into India — CRS vs FMCS schemes, documents, 7-step process & validity. Rego Services guide.

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7 Critical ISO 13485 Audit Mistakes Medical Device Manufacturers Must Avoid in India (2026 Guide)

Learn the 7 most common ISO 13485 audit mistakes that can lead to major nonconformities, certification delays, and CDSCO compliance issues.

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CDSCO Urological Medical Device License in India 2026

India's urological medical device market is rapidly expanding, making CDSCO licensing essential for manufacturers and importers.

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CCDSCO Registration for Class C Rehabilitation Medical Devices in India

Learn the complete CDSCO registration process for Class C rehabilitation medical devices in India. This 2026 guide covers MD9 licensing requirements, mandatory documentation, device classification, application procedures, regulatory compliance, and key steps manufacturers and importers must follow to legally market rehabilitation devices in India.

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CDSCO Oncology Medical Device License in India 2026: Complete Regulatory Guide

Get a complete overview of CDSCO licensing for oncology medical devices in India, including device classification, license requirements, documentation, and the SUGAM application process.

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How to Obtain a CDSCO Gynaecological Medical Device License in India 2026

Complete guide to CDSCO registration for gynaecological medical devices in India. Covers Class A–D devices, MD5, MD9, MD15 licenses, documents, fees, and compliance requirements.

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CDSCO Neurological Medical Device License in India 2026

A complete guide to CDSCO licensing for neurological medical devices in India. Learn about device classification (Class A–D), MD5, MD9 & MD15 license requirements, mandatory documentation, SUGAM portal application process, and compliance requirements for manufacturers and importers.

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CDSCO Nephrology Medical Device License in India 2026: Complete Compliance Guide

A complete guide to CDSCO approval for nephrology medical devices in India, including classification, licensing, documentation, application steps, and regulatory compliance requirements.

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CDSCO Classification of Radiology Medical Devices in India 2026

A comprehensive guide to CDSCO radiology device classifications, covering X-ray, MRI, ultrasound, nuclear medicine devices, risk categories, and licensing requirements in India.

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What is the CDSCO SUGAM Portal? How to Register

Complete 2026 guide to the CDSCO SUGAM portal — what it is, how to register step by step, divisions covered (drugs, medical devices, cosmetics, clinical trials), documents required, and how Rego Services supports your SUGAM submission — by Rego Services Pvt. Ltd.

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CDSCO Registration for PPE in India 2026

Understand PPE classification under MDR 2017, MD5 manufacturing license requirements, mandatory documentation, ISO 13485 compliance, and the complete SUGAM application process for obtaining CDSCO approval in India.

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CDSCO General Hospital Medical Device License in India 2026

Understand CDSCO medical device regulations for general hospital equipment in India. Learn about device classification, licensing pathways, documentation requirements, SUGAM portal applications, and compliance obligations under the Medical Devices Rules, 2017.

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CDSCO Registration for Pain Management Devices in India (2026)

Understand CDSCO classification, MD5 and MD9 licensing requirements, import regulations, documentation, fees, and the complete SUGAM application process for pain management medical devices in India.

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How to Start a CT Scan Manufacturing Business in India (2026 Complete Guide)

A step-by-step guide to launching a CT scanner manufacturing business in India, covering CDSCO Class C classification, MD9 manufacturing license requirements, regulatory approvals, documentation, compliance standards, and the complete SUGAM application process.

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How to Obtain a CDSCO License for BP Monitor Manufacturing in India

Everything manufacturers and importers need to know about Class B medical device compliance, licensing pathways, regulatory documentation, and approval requirements under MDR 2017.

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ECG Machine Manufacturing in India: Regulatory, Licensing & Business Setup Guide for 2026

A comprehensive guide covering ECG device manufacturing regulations, CDSCO approvals, ISO 13485 requirements, MD5 licensing, facility setup, documentation, and growth opportunities in India's expanding medical device sector.

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CDSCO Registration for ENT Medical Devices in India 2026: Complete Licensing & Compliance Guide

Learn how to obtain CDSCO approval for ENT medical devices in India. This comprehensive 2026 guide covers device classification (Class A–D), MD5, MD9 & MD15 licenses, required documents, fees, and the complete SUGAM registration process for manufacturers and importers.

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CDSCO Registration for Ophthalmic Medical Devices in India

Learn the CDSCO classification, MD5, MD9 & MD15 licensing requirements, documentation checklist, fees, and SUGAM application process for ophthalmic medical devices in India.

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CDSCO Operation Theatre Medical Device License in India 2026

Learn the CDSCO MD5, MD9, and MD15 license process for operation theatre medical devices — OT device classification, mandatory documents, application steps, validity, and compliance requirements under MDR 2017 in this complete 2026 guide

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CDSCO Medical Device Test License (MD13 & MD17) in India 2026

Learn the CDSCO MD13 and MD17 test license process, required documents, validity, and compliance requirements under MDR 2017 in this complete 2026 guide.

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Dermatological & Plastic Surgery Medical Devices in India 2026

Discover the complete CDSCO registration process for dermatological and plastic surgery medical devices in India.

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ISO 13485 Certification in India

Learn everything about ISO 13485 certification in India, including its importance for medical device manufacturers, CDSCO licensing requirements, key benefits, and the certification process.

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CDSCO Registration for Dental Medical Devices in India

Planning to manufacture, import, or sell dental medical devices in India? Understanding CDSCO regulations is essential for market entry and compliance.

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CDSCO License for Anaesthesia Medical Devices in India 2026

Class A to D classification, MD5 and MD9 pathways, fees, and the 8-step SUGAM process for anaesthesia device manufacturers and importers.

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Starting a Blood Collection Tube Manufacturing Business in India in 2026

Planning to manufacture blood collection tubes in India? Understanding the CDSCO regulatory framework is essential before setting up your facility.

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CDSCO License for Orthopaedic Medical Devices in India

Orthopaedic medical devices such as bone plates, screws, spinal implants, joint prostheses, and surgical instruments are regulated under India's Medical Device Rules (MDR) 2017.

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CDSCO Device Master File (DMF) Guide 2026

Complete guide to preparing a compliant Device Master File (DMF) for CDSCO medical device licensing in India.

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CDSCO License for Implantable Medical Devices in India 2026

Class C/D classification, MD9/MD15 pathways, and the 11-step SUGAM process for implant manufacturers and importers.

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CDSCO License for Manufacturing Thermometer in India 2026

Complete guide to CDSCO MD5 licensing for thermometer manufacturers in India, covering classification, documents, and the application process.

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CDSCO License for Manufacturing Glucometer in India 2026

Learn everything about obtaining a CDSCO license for manufacturing glucometers in India.

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How CDSCO Classifies Software as a Medical Device (SaMD) in India

Learn how CDSCO classifies Software as a Medical Device (SaMD) in India under MDR 2017.

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How to Prepare the CDSCO Risk Management File for SaMD in 2026

Complete guide to preparing a CDSCO-compliant SaMD Risk Management File, including ISO 14971, AI risk controls, cybersecurity, and regulatory documentation.

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How to Implement an Effective CDSCO Medical Device QMS in 2026

A complete guide to ISO 13485 compliance, QMS implementation, risk management, CAPA systems, and CDSCO inspection readiness.

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How to Prepare the CDSCO Plant Master File in 2026

Learn how to prepare an audit-ready CDSCO Plant Master File (PMF) for MD5 and MD9 applications.

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CDSCO Documentation For Medical Device Licensing in 2026

Complete Guide to DMF, PMF, CER & ISO 13485 Documentation

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CDSCO MD15 Import License in 2026: Procedure & Documents

Learn how to obtain the CDSCO MD15 import license for medical devices in India

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CDSCO MD9 Manufacturing License in 2026: Procedure & Documents

Learn how to obtain the CDSCO MD9 license for Class C and D medical devices.

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CDSCO MD5 Manufacturing License in 2026: Procedure & Documents

Learn the complete step-by-step process to obtain your CDSCO MD5 license for Class A and B medical devices.

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CDSCO Audit in 2026: Are You Ready?

Discover the critical compliance areas inspectors review and download the essential checklist to identify gaps before your next CDSCO audit.

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CDSCO Medical Device Registration 2026: Complete Compliance Guide

Explore the latest CDSCO registration requirements, risk-based audits, SaMD compliance, import licensing, and regulatory updates for medical devices in India.

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Navigating the Regulatory Seas

Stay updated on government compliance and product certification. Discover key regulatory changes, industry insights, and tips to stay compliant.

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Unlocking Excellence with BIS Certification

Explore the importance of BIS-CRS and ISI certifications and how our experts help you navigate the process with ease.

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Unlock Growth with GeM

Explore GeM registration & training to expand into government procurement with ease and expert support.

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EPR for Waste Management

EPR for Batteries, Plastic & E-Waste

Discover how Extended Producer Responsibility (EPR) can simplify compliance and boost sustainability efforts.

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Navigating CE Certification

Navigating CE Certification

Explore how CE Certification boosts product credibility and opens doors to EU & Indian markets.

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Maximizing Sustainability

Maximizing Sustainability

Learn how Rego Services helps reduce carbon footprints and navigate sustainability with ease.

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Pathway to Quality Assurance

Explore how ISO certification by Rego Services enhances quality, compliance, and global credibility.

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Guide to USFDA Compliance

Step into the US market confidently with expert guidance on USFDA safety, labeling, and regulatory standards.

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BIS Now Covers CCTV Cameras

MeitY mandates BIS registration for CCTV cameras to ensure security, quality, and compliance. Stay ahead with the latest update.

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Powering a Greener Tomorrow

India launches Star Labelling for solar modules via BEE to promote quality and energy-efficient products. Voluntary until 2025, mandatory after.

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Navigate WPC/ETA Certification with Ease

Discover how to effortlessly comply with India’s wireless tech regulations through WPC & ETA certifications. Ensure product safety and market readiness.

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Simplifying STQC Certification and Testing

Gain seamless access to markets with STQC certification. Learn how Rego Services supports your journey toward quality assurance and regulatory compliance.

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