Medical device regulations are constantly changing and evolving to better safeguard the health and safety of the public. However these regular changes may impact manufacturers with regards to their product requirements and registrations with local and overseas regulators.
At STC, our team of knowledgeable experts are up-to-date with the latest regulatory requirements in key markets to ensure that compliance is met and support medical device manufacturers in gaining market entry quickly.
Key Market Support
Our Medical Device Product Classification & Regulatory Support services include:
Biological Testing (ISO 10993)
For more information about our Medical Devices Testing services, please feel free to contact us.
Medical Devices Testing
LUCIDEON Medical Device Services
As part of our commitment to offering the most extensive services to our customers, STC is working in collaboration with LUCIDEON to provide a greater range of services including Medical Device Consultancy, Materials Developments and Technology Innovations. STC and LUCIDEON’s combined expertise in the healthcare industry can assist manufactures in advancing products quickly into the market and accelerate growth in this competitive landscape.
For more information about STC’s service via LUCIDEON please visit: