International Safety Standards & Manufacturing Guidelines for FCTI/LAB RMS Products

At the Physician Education Awareness Training held on 14th October 2019 in Kota Kinabalu, Malaysia, Prof. Dr. Mike Chan conducted a session on  International Safety Standards and Manufacturing Guidelines for FCTI/LAB RMS Products. 

His presentation provided a comprehensive overview of the regulatory frameworks, quality control measures, and industry best practices that ensure the safety, efficacy, and compliance of regenerative medicine products. Attendees gained valuable insights into the critical role of stringent manufacturing guidelines in maintaining product integrity, patient safety, and global market acceptance.

This training session equipped healthcare professionals and industry stakeholders with the essential knowledge required to navigate the complexities of regulatory compliance and implement high standards in the production and application of FCTI/LAB RMS products.