+91-7490017774 (For Enquiry Only) +91-7490017774 (For Enquiry Only) +91 9429952147 (For Career Only)
enquiry@mavenprofserv.com
Maven
Template
Bewildered by Regulatory Requirements?
Learn from the Experts

Blogs

  2. Blogs
Medical-Devices-Regulation
Apr 29, 2024

Maven

Medical Device Regulation for Custom-made Devices
MEDICAL-DEVICE-REGULATION-MDR
Apr 18, 2024

Maven

Comparison OF The Key Differences Between The MDR And IVDR In The EU
IVDRs-Summary-of-Safety-and-Performance
Apr 10, 2024

Maven

Ensuring Compliance: Understanding the IVDR’s Summary of Safety and Performance (SSP)
Packaging-Validation-1
Apr 3, 2024

Maven

What is Packaging Validation?
risk-management
Sep 26, 2023

Maven

The Importance of Risk Management for Medical Device Manufacturers
CEP
Aug 3, 2023

Maven

What is a Clinical Evaluation Plan and Why is it Important?
MEDICAL-DEVICE-MANUFACTUTRER
Jul 27, 2023

Maven

CE Mark for Medical Devices What You Need to Know to Stay Ahead in the Industry
Medical Device Regulation MDR
May 19, 2023

Maven

EN ISO 14971:2019/A11:2021 and EU MDR/IVDR Safety & Performance Requirements
(EU) 2017/745 and (EU) 2017/746
Jan 13, 2023

Maven

Amended Transition Timelines for EU MDR 2017/745 and IVDR 2017/746
EU IVDR Regulation
Dec 15, 2022

Maven

European Commission Considers Extending MDR and IVDR Deadlines

Tags

Recent Post

Performance Evaluation Report
June 30th, 2025

Why the Performance Evaluation Report (PER) Is Critical for IVDR Compliance
Technical Documentation
June 26th, 2025

Why It’s Crucial to Start Preparing Your IVDR Technical Documentation Now
EU IVDR Compliance
June 19th, 2025

How to Manage EU IVDR Compliance Challenges Effectively

Are You Looking For Medical Devices Certifications?

Contact Us