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 SULFATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of METAPROTERENOL SULFATE, including repackagers and relabelers. The FDA regulates METAPROTERENOL SULFATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. METAPROTERENOL SULFATE 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 SULFATE supplier is an individual or a company that provides METAPROTERENOL SULFATE active pharmaceutical ingredient (API) or METAPROTERENOL SULFATE finished formulations upon request. The METAPROTERENOL SULFATE suppliers may include METAPROTERENOL SULFATE API manufacturers, exporters, distributors and traders.
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A METAPROTERENOL SULFATE written confirmation (METAPROTERENOL SULFATE WC) is an official document issued by a regulatory agency to a METAPROTERENOL SULFATE manufacturer, verifying that the manufacturing facility of a METAPROTERENOL SULFATE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting METAPROTERENOL SULFATE APIs or METAPROTERENOL SULFATE finished pharmaceutical products to another nation, regulatory agencies frequently require a METAPROTERENOL SULFATE WC (written confirmation) as part of the regulatory process.
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