+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
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
EU MDR 2017
Nov 29, 2022

Maven

Quantification of Benefit – Risk Analysis
Assessment Procedures
Nov 23, 2022

Maven

The routes to conformity
Clinical Development Plan
Oct 11, 2022

Maven

Clinical Development Plan (CDP)
Medica device manufacturing
Oct 3, 2022

Maven

Identification and Traceability in Medical Device Industry

Tags

Recent Post

Medical Device Labeling Compliance
June 4th, 2025

Medical Device Labeling Compliance: How to Avoid Regulatory Pitfalls
Aseptic Processing
May 28th, 2025

Regulatory Innovations for Aseptic Processing: Adapting to Evolving Standards
Medical Device Recall
May 15th, 2025

Medical Device Recalls: Causes, Consequences, and Prevention

Are You Looking For Medical Devices Certifications?

Contact Us