Regulatory Research Solutions for Accessing International Markets
Gathering all regulatory market data at the earliest stages of your product development will help you identify and address potential impacts to your design. With our market research services, we can help to facilitate a smooth transition to testing, and ultimately a faster, less complicated certification process for you and your business.
- Identify local country requirements specific to your product
- Develop a customized regulatory strategy based on your priorities
Intertek does not provide consulting services for management systems certification. Any consulting activities provided by Intertek are separate and independent from certification activities.
Knowledge Center
Download the latest information from our medical device compliance experts
Creation of IEC 60601-1 4th Edition
IEC 60601-1-2 Ed. 4.1 Overview of Requirements
Medical OEM Wireless Coexistence Testing
Artificial Intelligence (AI) and Machine Learning (ML) in Medical Devices
Biocompatibility Risk Assessment and Evaluation Plans
For more expert papers, recordings, and presentations, visit our Medical Resources hub.
Related Links
- ETL Mark The Industry's Fastest Certification Program
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- Reese's Law – ANSI/UL 4200A-2023
- My Test Central
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- Certification Marks
- Global Research & Certification
- Medical Podcast - Compliance with Clarissa
- Satellite Client Test Program
- Planning for Quality through Disruptions
- Intertek's world-class team of Medical Experts
