Apex Healthcare Limited: ISO 9001:2008, WHO-GMP, US FDA-audited manufacturer & exporter of APIs, bulk drugs, and formulations.
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Apex Healthcare Limited: ISO 9001:2008, WHO-GMP, US FDA-audited manufacturer & exporter of APIs, bulk drugs, and formulations.
Registrant Name : Gapi Bio Co., Ltd.
Registration Date : 2025-06-23
Registration Number : 20250623-148-I-717-13
Manufacturer Name : Apex Healthcare Limited
Manufacturer Address : Plot No. - 4710, 4711, 4707-A/8, 4707-A/9, GIDC Industrial Estate, Ankleshwar, Dist.-...
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PharmaCompass offers a list of Meloxicam 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 Meloxicam manufacturer or Meloxicam supplier for your needs.
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A AC-1325 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AC-1325, including repackagers and relabelers. The FDA regulates AC-1325 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AC-1325 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of AC-1325 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AC-1325 supplier is an individual or a company that provides AC-1325 active pharmaceutical ingredient (API) or AC-1325 finished formulations upon request. The AC-1325 suppliers may include AC-1325 API manufacturers, exporters, distributors and traders.
click here to find a list of AC-1325 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a AC-1325 Drug Master File in Korea (AC-1325 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of AC-1325. The MFDS reviews the AC-1325 KDMF as part of the drug registration process and uses the information provided in the AC-1325 KDMF to evaluate the safety and efficacy of the drug.
After submitting a AC-1325 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 AC-1325 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of AC-1325 suppliers with KDMF on PharmaCompass.
We have 11 companies offering AC-1325
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