Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1Supriya Lifescience Ltd
02 2Supriya Lifescience Ltd.
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : 아이엠씨디코리아주식회사
Registration Date : 2024-09-11
Registration Number : 20210302-211-J-852(2)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC Tal-Khed. Dist-Ratnagiri, Maharashtra, Pi...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2021-03-02
Registration Number : 20210302-211-J-852
Manufacturer Name : Supriya Lifescience Ltd
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC Tal-Khed. Dist-Ratnagiri, Maharashtra, Pi...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : Daeshin Pharmaceutical Co., Ltd.
Registration Date : 2021-12-06
Registration Number : 20210302-211-J-852(1)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC Tal-Khed. Dist-Ratnagiri, Maharashtra, Pi...
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A Polargen TD manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Polargen TD, including repackagers and relabelers. The FDA regulates Polargen TD manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Polargen TD API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Polargen TD supplier is an individual or a company that provides Polargen TD active pharmaceutical ingredient (API) or Polargen TD finished formulations upon request. The Polargen TD suppliers may include Polargen TD API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Polargen TD Drug Master File in Korea (Polargen TD KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Polargen TD. The MFDS reviews the Polargen TD KDMF as part of the drug registration process and uses the information provided in the Polargen TD KDMF to evaluate the safety and efficacy of the drug.
After submitting a Polargen TD KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Polargen TD API can apply through the Korea Drug Master File (KDMF).
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