Regulatory
Consulting
K&C Associates was founded in 2005 to assist medical device companies with business development and Taiwan Food and Drug Administration (TFDA) registration issues.
We assist medical device companies with Taiwan regulatory strategy, manufacturer registration, medical device registration, in-country regulatory representation, reimbursement application, Good Distribution Practice (GDP) consulting, and any other regulatory services.
We can assist you in solving regulatory issues and acting as your guide in navigating the Taiwan market.
Why Choose Us?
K&C Associates provides comprehensive
medical device consulting services
With over 18 years of experience, K&C has the knowledge, expertise, and resources to ensure success.
Services include TFDA registration assistance, project strategy determination, intellectual property protection, and ongoing support.
K&C has helped over 300 companies and completed more than 1,500 registrations.
