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USP-MHLW/PMDA Joint Workshop - Registration started. July 11, 2024. RS. Recent Publications by PMDA Staff updated. July 9, 2024. Safety. MHLW Pharmaceuticals and Medical Devices Safety Information No.411 posted. July 9, 2024. Events. Call for PMDA-ATC Herbal Medicine Review Seminar 2024 has been opened. July 9, 2024. Int. Seminar schedule has been updated. Back number. Currently, there is no applicable information. Back number. July 17, 2024.
The Pharmaceuticals and Medical Devices Agency (独立行政法人医薬品医療機器総合機構, Dokuritsu-gyōsei hōjin iyakuhin-iryō-kiki-sōgō-kikō) (PhMDA ...
3 days ago · Haryana, announced the constitution of the Panchkula Metropolitan Development Authority (PMDA) for swift execution of the region’s integrated development plan in June 2021. On the last day of Haryana Vidhan Sabha’s monsoon session, in August 2021, the legislative body passed the Panchkula Metropolitan Development Authority (PMDA) Bill, making Panchkula the third city after Gurugram and Faridabad to get such an institution.
For information about PMDA, please visit here. Recent Press Releases. APEC endorsed Japan’s PMDA as a pilot Training Center for Medical Devices Regulation (March 18, 2019) To protect people from drug abuse. For Travelers. Illicit Drugs[PDF:748KB] Cannabis[PDF:902KB] To see the charts(pdf file), it requires a software "Acrobat Reader". You can get Acrobat Reader for free, please click on the next button.
Apr 29, 2023 · The PMDA was established in April 2004 as a result of the merger between the Pharmaceutical Affairs Agency (PAA) and the National Institute of Health Sciences (NIHS). The PMDA is responsible for ...
Aug 12, 2018 · For the most comprehensive and detailed overview of the Japanese medical device regulations, view the Japan Medical Device Regulations Webcast.Key topics include PMDA consultations, device classification, Foreign Manufacturer Registration, Japanese GCP, product reimbursement, how to expedite product registration and maximize the use of foreign clinical data, and more.
Sai Life Sciences is a full-service CRO / C,DMO (contract research, development and manufacturing organization) driven by a vision to support the launch of 25 new medicines by 2025.
PMDA Medical Safety Information. Procedures in Japan. Master File System. Accreditation of Foreign Manufacturers. Advanced efforts. Science Board. Subcommittee on Placebo-controlled Studies. Subcommittee on Non-clinical Studies. Pharmaceuticals Subcommittee. Bio-products Subcommittee. Advanced Review with Electronic Data Promotion Group. Strategy of SAKIGAKE by MHLW. Projects Across Multi-Offices in PMDA. JCN 3010005007409;
Apr 15, 2020 · The PMDA’s office of biologicals provides consultations concerning clinical trials of new biologic drugs and handles biotechnology medicines, which includes biosimilars. Requirements for biologic drugs differ from general drugs and depend on whether a biological product is a regenerative medicine product or not.
What's New Notice regarding Guidance for approval Covid-19 vaccine in India for restricted use in emergency situation which are already approved for restricted use by US FDA EMA, UK MHRA, PMDA Japan or which are listed in WHO Emergency use listing 15th April,2021 DCGI Message 202101 Jan 2021 For Medical devices which are under voluntary registrations, the file number generated is the registration number of firm. E-GOV cell at CDSCO CDSCO,HQ accredited with Quality Management Systems IS/ISO ...
