Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1Supriya Lifescience Ltd.
02 1BAKUL PHARMA PRIVATE LIMITED
03 1Bajaj Healthcare Limited (Unit-2)
04 5CSPC Innovation Pharmaceutical co.,ltd
05 1Jilin Province Shulan Synthetic Pharmaceutical Co., Ltd_x000D_
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : Hiple Co., Ltd.
Registration Date : 2017-11-28
Registration Number : 20171128-205-I-525-02
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC, Taluka - Khed, District - Ratnagiri, Mah...
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PharmaCompass offers a list of Theobromine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Theobromine manufacturer or Theobromine supplier for your needs.
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A Tox21_300016 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300016, including repackagers and relabelers. The FDA regulates Tox21_300016 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300016 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 Tox21_300016 supplier is an individual or a company that provides Tox21_300016 active pharmaceutical ingredient (API) or Tox21_300016 finished formulations upon request. The Tox21_300016 suppliers may include Tox21_300016 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 Tox21_300016 Drug Master File in Korea (Tox21_300016 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Tox21_300016. The MFDS reviews the Tox21_300016 KDMF as part of the drug registration process and uses the information provided in the Tox21_300016 KDMF to evaluate the safety and efficacy of the drug.
After submitting a Tox21_300016 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 Tox21_300016 API can apply through the Korea Drug Master File (KDMF).
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