Tag Archive for: device classification
CHINA AMENDS MEDICAL DEVICE APPLICATION SUBMISSION PROCESS
/in China, Latest Updates/by Bryan GilburgIn an ongoing effort to refine and improve the systems and procedures for medical device registration in China, the National Medical Products Administration or NMPA (previously the CFDA) moved to a new on-line submission system and harmonized the applications table of contents to international standards.
INDONESIA ENFORCES MEDICAL DEVICE LABELING REQUIREMENTS
/in Indonesia, Latest Updates/by Bryan GilburgTHAI FDA ADDS ‘CONCISE EVALUATION’ FOR QUALIFYING MEDICAL AND IVD DEVICES
/in Latest Updates, Thailand/by Bryan GilburgNEW OFFICE SPACE FOR ASIA ACTUAL PHILIPPINES
/in Latest Updates, Philippines/by Bryan GilburgAsia Actual is excited to announce the dedication of our new office space in the Philippines. The investment reflects the company’s commitment to the Philippines market and expectations for growth.
INDIA TO REQUIRE REGISTRATION OF ALL CURRENTLY NON-NOTIFIED DEVICES
/in India, Latest Updates/by Bryan GilburgManufacturers of non-Notified medical devices are advised to evaluate their products of interest for India and begin to build their application files for a Registration Certificate
INDIA POSTPONES REGISTRATION DEADLINES FOR MOST NEWLY NOTIFIED MEDICAL DEVICES
/in India, Latest Updates/by Bryan GilburgPHILIPPINES OFFICIALLY LAUNCHES NEW MEDICAL DEVICE REGULATIONS
/in Latest Updates, Philippines/by Bryan GilburgNew medical device regulations in the Phillipines have been launched. Class A, Class B, Class C, and Class D medical devices will all be affected.
THAILAND ELEVATES REGULATORY STATUS OF BREAST IMPLANTS
/in Latest Updates, Thailand/by Bryan GilburgWith Regulation B.E. 2562 (revision from regulation B.E. 2540), the Thai FDA increased the regulatory status of breast implants from Notified to Licensed (Class 4)
HONG KONG ADVANCES TOWARDS MANDATORY MEDICAL DEVICE REGISTRATION
/in Latest Updates, Thailand/by Bryan GilburgHong Kong’s Department of Health officially changed the name of the Medical Device Control Office (MDCO) to the Medical Device Division (MDD) at the end of 2019.
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