Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
01 1Syn-Tech Chem & Pharm Co., Ltd.
02 1M/s Apotex Pharmachem India Pvt Ltd
03 1M/s CIpla Limited
04 1M/s Emcure Pharmaceuticals Limited
05 1M/s Glenmark Life Sciences Limited
06 1M/s Hetero Drugs Limited
07 2M/s Natco Pharma Limited
08 1M/s Nosch Labs Pvt Ltd
09 1M/s SMS Pharmaceuticals Limited
10 1M/s Sun Pharmaceuticals Industries ltd
11 1M/s Tianish Laboratories Privte Lmited
12 1M/s Unichem Laboratories Limited
13 1M/s. Apitoria Pharma Private Limited
14 1M/sMacleods pharmaceuticals Limited
15 1M/sUnimark Remedies Limited
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Date of Issue : 2022-02-22
Valid Till : 2025-07-15
Written Confirmation Number : TFDA-0002291
Address of the Firm : No. 168, Kai Yuan Rd, Hsin-Ying, Tainan City 73055, Taiwan
85
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A rizatriptan, benzoate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of rizatriptan, benzoate, including repackagers and relabelers. The FDA regulates rizatriptan, benzoate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. rizatriptan, benzoate 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 rizatriptan, benzoate supplier is an individual or a company that provides rizatriptan, benzoate active pharmaceutical ingredient (API) or rizatriptan, benzoate finished formulations upon request. The rizatriptan, benzoate suppliers may include rizatriptan, benzoate API manufacturers, exporters, distributors and traders.
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A rizatriptan, benzoate written confirmation (rizatriptan, benzoate WC) is an official document issued by a regulatory agency to a rizatriptan, benzoate manufacturer, verifying that the manufacturing facility of a rizatriptan, benzoate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting rizatriptan, benzoate APIs or rizatriptan, benzoate finished pharmaceutical products to another nation, regulatory agencies frequently require a rizatriptan, benzoate WC (written confirmation) as part of the regulatory process.
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