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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)
LUCIDEON Medical Device Services