Skip to content

admin@morulaa.com

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

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

Search

Navigating UK MDR Post‑Market Surveillance: Practical Differences from EU MDR and Actionable Morulaa Tips

PMS and Other Compliance

UK MDR Post-Market Surveillance

Navigating UK MDR Post‑Market Surveillance: Practical Differences from EU MDR and Actionable Morulaa Tips

The UK’s post‑Brexit amendments to post‑market surveillance (PMS) bring new

Simplifying FDA Adverse Event Reporting: Everything You Need to Know About Form 3500A

1. Introduction to the FDA Form 3500A: FDA Form 3500A

legal metrology act

Legal Meteorology Requirements, Medical Devices, India

Legal Metrology Compliance Are you a manufacturer or importer of

E-Waste Management for Medical Devices

E-Waste Management for Medical Devices in India

E-Waste Management for Medical Devices in India is crucial for

Pricing Framework Reforms: Drugs and Medical Devices, India

India Drug Pricing Reforms: New Framework and its Impact

Currently, the NPPA follows the regulations which are outlined in

PSUR India, CDSCO's Online Submission Requirement

PSUR India, CDSCO’s Online Submission Requirement

PSUR – Periodic Safety Update Reports The Central Drugs Standard

Guidelines on Recall System for Drugs, India

CDSCO Drug Recall Guidelines: Ensuring Compliance and Safety

This article referring to CDSCO/RRAS Ver.:00 dated 23/11/2012, talks about

Periodic Safety Update Reports: CDSCO's New Update

Periodic Safety Update Reports: CDSCO’s New Update

Periodic Safety Update Reports (PSURs) submission process has significantly undergone

Drugs & Cosmetics Act and PWM: Effects on Medical Devices

Drugs & Cosmetics Act and PWM: Effects on Medical Devices

The Drugs & Cosmetics Act of 1940, underpinning the regulatory

Price Capping in India by NPPA

The National Pharmaceutical Pricing Authority (NPPA) in India is a regulatory body responsible

« Previous Page1 Page2 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

Address

Morulaa HealthTech Pvt Ltd

38, Rajeshwari St, Santhosh Nagar,
Kandhanchavadi, Perungudi, Chennai, Tamil Nadu- 600096, India

Contact Us Today

Medical Device Regulatory Consultants

Market Research
Register Your Medical Device
Documents required
Authorized Agent
Import to India
Medical Device Registration in India | Complete Guide for Overseas Manufacturers

Market Research
Register Your Medical Device
Documents required
Authorized Agent
Import to India
Medical Device Registration in India | Complete Guide for Overseas Manufacturers

Let's Connect

About Us
Contact Us
Products
Blogs
News

About Us
Contact Us
Products
Blogs
News

© 2025 All Rights Reserved.

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?

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?