Regulatory consulting services supporting medical device and IVD manufacturers through CE marking, FDA 510(k) clearance, and UKCA certification processes. Includes technical documentation preparation, conformity assessment, risk management, and audit support for EU MDR, EU IVDR, and UK regulatory co...
Manufactured by
Maven Profcon Services LLP
Ahmedabad, India
We are a medical and IVD device regulatory consultancy that was established in 2016 and ever since we have been offering a wide array of services to the medical device fraternity to meet their regulatory needs. Our services include both holistic and customized solutions where we provide clients with end-to-end support for their certification requirements and also offer customized support if they are looking for specific documentation/services support instead of an entire submission. Our services include but are not limited to - CE - USFDA - UKCA - ISO 13485 - MDSAP - 21 CFR Part 820 - Clinical Trials - Country Registrations - Authorised Representative services (EC REP, UKRP, US agent, Swiss Rep) - UDI support - Annual Maintenance Services - Premium Organisational Maintenance Services - Clinical Evaluation writing and many more We have assisted more than 350 manufacturers with various certification requirements and our clients are based all around the globe.
✦ Product-Specific Coverage
Based on AI-matched alternatives related to this product across Suplivia's medical sourcing network.
Generated for this product
AI-matched supplier coverage based on related product alternatives.
ROOSON Consulting Service Co. Ltd
China · 2 relevant products
Red Medtech Ltd.
United Kingdom · 1 relevant product
WQS Management Consultants Inc.
United States · 3 relevant products
62 more relevant manufacturers available
Get free access to all relevant manufacturers for this product.
See all manufacturers →13 more sourcing countries available
Get free access to all sourcing countries identified for this product.
See all countries →See the full supplier coverage for this product
Get free access to all relevant manufacturers, sourcing countries, and product alternatives.
✓ Free for medical industry professionals.
from other manufacturers
from other manufacturers
3 of 94 closest product alternatives
ROOSON Consulting Service Co. Ltd · China
Regulatory consulting services for medical device market access, including clinical trial design, registration support, quality management system development, and international certification guidance for manufacturers seeking approval in China and global markets.
Red Medtech Ltd. · United Kingdom
Our experienced consulting team provides assistance in achieving and maintaining Europe CE mark certification, UKCA mark, FDA 510(k) clearances, and PMA approvals.
WQS Management Consultants Inc. · United States
Regulatory consulting service guiding medical device manufacturers through EU MDR compliance, CE certification, ISO 13485 quality management systems, and technical documentation requirements for market authorization.
91 more product alternatives available
Create a free account to compare more product alternatives and supplier options.
© 2026 Suplivia · Home · Browse Products