Time to market starts with trusted partnership, and for more than 50 years Keyworld has been partnering with manufacturers to provide global Medical Device certification, testing, inspection and assurance solutions.
Bring your Medical Device to market with a partner who can navigate Regulatory Requirements for IEC 60601-1, IEC 60601-1-2, MDR, IVDD, and the CB Scheme.
Reach your target markets quickly and cost-effectively with Electrical, Electromagnetic Compatability (EMC), Bluetooth and Wireless Testing, Cyber Security, Software and Mobile Application testing and certification for your medical device.
We fully support the medical device industry to comply with changing global Health and Environmental regulatory requirements and restrictions, such as RoHS, REACH and WEEE.
Medical device and materials testing including safety assessment through Extractables and Leachables and bioanalysis supporting all stages of development and manufacturing.
Multi-disciplined clinical teams who provide robust, GCP and ISO 14155 compliant clinical trials for low risk medical devices.
For Medical Products entering the Canadian Market, SPE-3000 serves as the model code for the field evaluation of medical electrical equipment (MEE) and medical electrical systems (MES), specifically pertaining to safety from electric shock, fire and mechanical hazards.
You benefit from our experience in delivering effective solutions to the complex global supply chains of some of the world’s biggest corporations.
You benefit from every innovation, whether it involves a simple extension to our Air and Ocean Freight products, whether it means a development in warehousing.
All of which explains why you’ll find the team of outstanding support at TransCargo ready to apply their passion for solutions in support of your business.
