Regulatory registration and compliance service for medical devices and biologics across NMPA (China), CE (Europe), and FDA (US) markets. Provides integrated support including preclinical research, testing, regulatory strategy, and clinical trial coordination to facilitate device approval and market ...
Manufactured by
Suzhou Yipin Quality Technical Service Co., Ltd
China
EPIN is a government-backed medical device technical service platform providing testing and contract research organization (CRO) services for medical devices and biopharmaceuticals. The company operates laboratories accredited by CNAS, CMA, US FDA GLP, and ILAC ISO 17025, serving China, US, and European markets. Services include electrical safety testing, EMC compatibility, animal studies, biocompatibility, sterilization validation, package aging, chemical characterization, risk analysis, finite element analysis, software evaluation, usability engineering, and clinical evaluation.
✦ 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.
EUCEREP B.V.
Netherlands · 2 relevant products
Maven Profcon Services LLP
India · 14 relevant products
P&L Scientific Inc.
United States · 2 relevant products
68 more relevant manufacturers available
Get free access to all relevant manufacturers for this product.
See all manufacturers →12 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 116 closest product alternatives
EUCEREP B.V. · Netherlands
Regulatory representation and compliance service enabling non-EU manufacturers to obtain EU Authorized Representative (EAR) and UK Responsible Person (UKRP) status for medical device market access. Supports CE marking, EUDAMED registration, technical documentation, and Quality Management System establishment to meet European and UK regulatory requirements.
Maven Profcon Services LLP · India
Regulatory consulting services supporting medical device and IVD manufacturers through CE marking, US FDA 510(k) clearance, and UKCA certification. Services include technical documentation preparation, conformity assessment, clinical evaluation, risk management, and audit support to ensure compliance with EU MDR, EU IVDR, and UK regulatory requirements.
P&L Scientific Inc. · United States
Regulatory affairs consulting service specializing in China NMPA (National Medical Products Administration) compliance and medical device registration. Supports manufacturers in navigating Chinese regulatory pathways, documentation preparation, and market approval processes for medical devices.
113 more product alternatives available
Create a free account to compare more product alternatives and supplier options.
© 2026 Suplivia · Home · Browse Products