079-40026222 +91-7490017774 +91-7490017774

business@mavenprofserv.com

Who We Are
Services
Pricing
RegXpert
- Blog
- Events
- Career
- Testimonials
Contact Us

admin@mavenprofserv.com
079-40026222
+91-7490017774

Search for:

Template

Month: January 2023

Amended transition timelines of Regulations (EU) 2017/745 and (EU) 2017/746

Posted on January 13, 2023May 19, 2023 by Maven Profserv

Posted in Medical DeviceLeave a Comment on Amended transition timelines of Regulations (EU) 2017/745 and (EU) 2017/746

Search

Recent Posts

The Importance of Risk Management for Medical Device Manufacturers
What is a Clinical Evaluation Plan and Why is it Important?
CE Mark for Medical Devices What You Need to Know to Stay Ahead in the Industry
Unraveling the Relationship between EN ISO 14971:2019/A11:2021 and the General Safety and Performance Requirements of Regulation (EU) 2017/745 & 2017/746
Amended transition timelines of Regulations (EU) 2017/745 and (EU) 2017/746

Recent Comments

No comments to show.

Archives

September 2023
August 2023
July 2023
May 2023
January 2023
December 2022
November 2022
October 2022
August 2022
June 2022
May 2022
April 2022
September 2021
August 2021
July 2021

Categories

Cosmetic
Covid-19
Medical Device
Uncategorized

Maven Profcon Services LLP is a service provider for Consultation, Audits, Trainings, GAP audits, Conformity Assessments, Various Evaluation, Documents Review & Testing. Supported with the team of Management Graduates, Engineering Graduates, Technical experts, Subject experts, Trainers and lead auditors.

Home
Who We Are
Pricing
Blog
Contact Us
Templates

Services

Europe

INDIA

USA

UK

OTHERS

Europe

Medical Device CE Marking
IVD CE Marking
PPE CE Marking
Software CE Marking
EN ISO 13485
Technical Documentation
Clinical Evaluation
Risk Management File
Medical Device Testing
PMS+PMCF+PMSR+PSUR
SSCP
EUDAMED Registration / SRN
UDI
EU Registration or Device Registration
European Authorized Representative
Liability Insurance
European Free Sale Certificate

INDIA

Medical Device Rules 2017K
Test License
Plant Approval
Manufacturing License
Import License
Post-approval changes
Free Sales Certificate
Device Master File
Clinical Investigation

USA

US FDA 510K
NIOSH
Establishment Registration and Device Listing
US Agent Service
FDA Label Review
Food Registration
Drug Registration
Cosmetic Registration

UK

UKCA MARK
UK RESPONSIBLE PERSON
BS EN ISO 13485
MHRA Registration

OTHERS

Country Registration
MDSAP
Annual Maintenance Contract
Turnkey Projects
Internal Quality Audit
Management Review Meeting
Training
Validation
IQMS
ISO 13485
ISO 9001 & ISO 13485 – IQMS

JOIN OUR NEWSLETTER

Sign up to receive a monthly email on the latest updates, features, and news!

Address

Maven Profcon Services LLP

1215 & 1216, Iconic Shyamal, Shyamal Cross Road, Ahmedabad – 380015, Gujarat, India.

690 Little Grey St, Unit 134, London, ON N5Z 4M9, Canada

contact

business@mavenprofserv.com enquiry@mavenprofserv.com
079-40026222
079-40046222
+91-7490017774
+1 226 998 0460

Copyright © 2023 Maven Profcon Services LLP

Privacy Policy
Cookies Policy
Disclaimer

Design With heart By Pixielit Studios