Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1Aarti Pharmlabs Limited
02 1Cipla Limited
03 1Dynamit Nobel GmbH Explosivstoff and Systemtechnik
04 1Micronisierungs-Kontor-Oberrot GmbH
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Registrant Name : Sangjin Corporation
Registration Date : 2016-01-22
Registration Number : No. 6580-23-ND
Manufacturer Name : Aarti Pharmlabs Limited
Manufacturer Address : Plot No: E - 50, 50/1 & 59/1, Unit – IV, MIDC, Tarapur, Taluka & District: Palghar,...
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PharmaCompass offers a list of Ciclesonide 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 Ciclesonide manufacturer or Ciclesonide supplier for your needs.
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A BY-9010 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BY-9010, including repackagers and relabelers. The FDA regulates BY-9010 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BY-9010 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 BY-9010 supplier is an individual or a company that provides BY-9010 active pharmaceutical ingredient (API) or BY-9010 finished formulations upon request. The BY-9010 suppliers may include BY-9010 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 BY-9010 Drug Master File in Korea (BY-9010 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of BY-9010. The MFDS reviews the BY-9010 KDMF as part of the drug registration process and uses the information provided in the BY-9010 KDMF to evaluate the safety and efficacy of the drug.
After submitting a BY-9010 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 BY-9010 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of BY-9010 suppliers with KDMF on PharmaCompass.
We have 4 companies offering BY-9010
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