Client Impact Stories
We work with medical device and in vitro diagnostic clients who operate globally around the world offering fresh approaches to the issues that matter most to them.
Through a rigorous analysis of each client’s individual situation, we develop customized solutions that align with the overall business objectives, create value, and deliver sustainable advantage. Whether you are a company needing one-off consulting assistance or a medical device manufacturer that requires in-depth project management, Intertek provides both short-term and long-term consulting solutions to meet your exact needs either on an a la carte basis or at a fixed price guarantee.
Overcoming Regulatory Compliance Challenges to Achieve Market Success
In this case study for medical devices, learn how Intertek helped a global medical device manufacturer faced with a competitive threat streamline its product development process reducing its time to market by 50%.
Reducing time to Market by Streamlining the Product Development Process
In this case study focusing on laboratory equipment we are breaking the Cycle of Product Testing Failures and Re-designs to Achieve Certification. Find out how Intertek helped an entrepreneurial manufacturer of a revolutionary hospital disinfectant system trapped in a cycle of product testing failures and re-designs, achieve certification and get to market on schedule and within budget.
TransMotion Medical Video
"We're in a competitive landscape, and we need to be out there in front of our competitors. Having somebody that we can rely on to increase the speed of our project work is important... I can lean on the people at Intertek to help guide me through the technical aspects of what needs to be accomplished."
Intertek does not provide consulting services for management systems certification. Any consulting activities provided by Intertek are separate and independent from certification activities.
- Evolution of the Home Healthcare Market and Medical Device Compliance
White Paper | Webinar Recording
- Ventilator Production: Introductory Guide to Regulatory Requirements
- Critical Care Medical Devices: First-In-Queue Priority
- Medical Robots Fact Sheet
- Product Listing & Marking Strategies White Paper
- IEC 60601-1-2 Edition 4 White Paper
- Updated FCC Approval Process Webinar
- Extractables and Leachables Studies Fact Sheet
- Five Steps to Medical Device Commercialization in the United States White Paper
- Making Green Profitable: Using IEC 60601-1-9 as a Competitive Advantage White Paper
- ETL Mark The Industry's Fastest Certification Program
- Search and Buy Medical Device Standards
- My Test Central
- Certification Marks
- Global Research & Certification
- Medical Podcast - Compliance with Clarissa
- Satellite Data Acceptance Program
- Planning for Quality through Disruptions
- Intertek's world-class team of Medical Experts
- Intertek Protek - The world’s first industry-agnostic, end-to-end health, safety and wellbeing assurance program