Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
01 1Syn-Tech Chem & Pharm Co., Ltd.
01 1Orciprenaline Sulfate
01 1TFDA-0002291
01 1Taiwan
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
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A Metaproterenol Hemisulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metaproterenol Hemisulfate, including repackagers and relabelers. The FDA regulates Metaproterenol Hemisulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metaproterenol Hemisulfate 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 Metaproterenol Hemisulfate supplier is an individual or a company that provides Metaproterenol Hemisulfate active pharmaceutical ingredient (API) or Metaproterenol Hemisulfate finished formulations upon request. The Metaproterenol Hemisulfate suppliers may include Metaproterenol Hemisulfate API manufacturers, exporters, distributors and traders.
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A Metaproterenol Hemisulfate written confirmation (Metaproterenol Hemisulfate WC) is an official document issued by a regulatory agency to a Metaproterenol Hemisulfate manufacturer, verifying that the manufacturing facility of a Metaproterenol Hemisulfate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Metaproterenol Hemisulfate APIs or Metaproterenol Hemisulfate finished pharmaceutical products to another nation, regulatory agencies frequently require a Metaproterenol Hemisulfate WC (written confirmation) as part of the regulatory process.
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