1. Service DescriptionWhen a list of non-conformities is given after the external audit, we can make a corrective action plan based on it.The GMP consulting team of Tigermed-Jyton Group can provide:Customized writing for single processes;Preparation of the system correction plan;Preparation of
1. Overview of Manufacturing and Testing Environment and Relevant EquipmentClean rooms are essential for the production of sterile/implantable medical devices and IVD reagents. The control level of environment and equipment in them directly influences the quality of medical devices. Tigermed-Jyton M
Simulated assessment: At the first registration stage of the medical device, we perform a simulated assessment for the factory before on-site assessment by the NMPA assessor. It is an in-process service to find out and fix any possible problem in advance. It is generally needed before product market
1. OverviewIn accordance with Good Manufacturing Practice(GMP) and Good Supply Practice(GSP), the enterprise should establish and improve a Quality Management System which is applicable to the medical devices manufactured and operated and guarantee its effective operation based on releva
Production License OverviewIn accordance with Regulations on the Supervision and Administration of Medical Devices (No.650 Decree of the State Council of the People’s Republic of China), on the premise of conditions specified for medical device production, manufacturers of Class II and III medical
1. Service OverviewIn accordance with the Notice on Extending Pilot Work of the Medical Device Registrant System(G.Y.J.X.Z.[2019] No.33) issued by the NMPA, we are dedicated to promote the pilot work of the medical device registrant system. Our services can solve practical difficulties faced b
