Skip to content

admin[@]morulaa[dot]com

<img width="173" height="74" src="https://i0.wp.com/morulaa.com/wp-content/uploads/2024/08/morulaalogo.webp?fit=173%2C74&ssl=1" class="attachment-full size-full wp-image-24274" alt="" />

Market Data
Register
Distribute
Knowledge Process Outsourcing
AI – Based Registration
Blog
About Us
Contact Us

Menu

Market Data
Register
Distribute
Knowledge Process Outsourcing
AI – Based Registration
Blog
About Us
Contact Us

Search

Search

Close this search box.

Testing and Evaluation for Medical Devices/ IVD’s , India

Home » MDR india

Home » MDR india

MDR india

Medical device testing

Testing and Evaluation for Medical Devices/ IVD’s , India

On May 29, 2024, the Central Drugs Standard Control Organisation

Medical device labeling

Medical Device Labeling Requirements in India

Labeling for medical devices in India is very important for

MD-15 Import License, India

MD-15 Import License, India

MD-15 Import License: In the constantly evolving regulatory landscape of

FAQs by CDSCO: Key Highlights and Updates

FAQs by CDSCO: Key Highlights and Updates

Learn More About CDSCO Medical Device Registration Process This article

Class A Non-sterile/measured medical device

Exemption of Class A Non-Sterile/Non-Measuring Medical Devices from Licensing Regime

Introduction This Article deals with Class A Non-Sterile/Measuring Medical Devices

Voluntary Registration - Non-Notified Medical Devices

Voluntary Registration of Medical Devices in India

Introduction – Voluntary / Non-Notified Registration of Medical Devices in

Medical Device Amendment for Non-Notified Devices - Anesthesiology

Medical Devices Amendments Given By CDSCO

This article deals with various amendments which happened in the

Indian MDR - Deadline Approaching for Non-Notified Medical Devices

Indian MDR – Deadline Approaching for Non-Notified Medical Devices

Introduction : Indian MDR – Deadline Approaching for Non-Notified Medical

Medical Device Amendments

Medical Device Amendments

Medical Device Amendments

Regulatory, Medical device rules 2017

Medical Device Rules India, 2017: Classification of Medical Devices Regulations and Regulatory Approval for Registration

The classification of medical devices rules along with regulatory approval and registration

« Previous Page1 Page2 Page3 Next »

Category

CDSCO
CDSCO Amendments
Classification
Cosmetics
Document Requirements
Drugs
Import
India Market
In-vitro Diagnostics
Labelling
PMS and Other Compliance
Registration India
Software as Medical Device
SUGAM
Timeline
India Market

All rights reserved

<img width="173" height="74" src="https://i0.wp.com/morulaa.com/wp-content/uploads/2024/08/morulaalogo.webp?fit=173%2C74&ssl=1" class="attachment-full size-full wp-image-24274" alt="" />

Let’s Talk

Request your free proposal. Call us today, or fill out the form and we will get right back to you!

Interested In?