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 Dom-meloxicam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dom-meloxicam, including repackagers and relabelers. The FDA regulates Dom-meloxicam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dom-meloxicam 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 Dom-meloxicam supplier is an individual or a company that provides Dom-meloxicam active pharmaceutical ingredient (API) or Dom-meloxicam finished formulations upon request. The Dom-meloxicam suppliers may include Dom-meloxicam 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 Dom-meloxicam Drug Master File in Korea (Dom-meloxicam KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Dom-meloxicam. The MFDS reviews the Dom-meloxicam KDMF as part of the drug registration process and uses the information provided in the Dom-meloxicam KDMF to evaluate the safety and efficacy of the drug.
After submitting a Dom-meloxicam 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 Dom-meloxicam API can apply through the Korea Drug Master File (KDMF).
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