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 Omnaris HFA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Omnaris HFA, including repackagers and relabelers. The FDA regulates Omnaris HFA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Omnaris HFA 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 Omnaris HFA supplier is an individual or a company that provides Omnaris HFA active pharmaceutical ingredient (API) or Omnaris HFA finished formulations upon request. The Omnaris HFA suppliers may include Omnaris HFA 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 Omnaris HFA Drug Master File in Korea (Omnaris HFA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Omnaris HFA. The MFDS reviews the Omnaris HFA KDMF as part of the drug registration process and uses the information provided in the Omnaris HFA KDMF to evaluate the safety and efficacy of the drug.
After submitting a Omnaris HFA 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 Omnaris HFA API can apply through the Korea Drug Master File (KDMF).
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We have 4 companies offering Omnaris HFA
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