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 : 2026-12-31
Written Confirmation Number : TFDA-0002291
Address of the Firm : No. 168, Kai Yuan Rd, Hsin-Ying, Tainan City 73055, Taiwan
75
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A Orciprenaline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Orciprenaline, including repackagers and relabelers. The FDA regulates Orciprenaline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Orciprenaline 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 Orciprenaline supplier is an individual or a company that provides Orciprenaline active pharmaceutical ingredient (API) or Orciprenaline finished formulations upon request. The Orciprenaline suppliers may include Orciprenaline API manufacturers, exporters, distributors and traders.
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A Orciprenaline written confirmation (Orciprenaline WC) is an official document issued by a regulatory agency to a Orciprenaline manufacturer, verifying that the manufacturing facility of a Orciprenaline active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Orciprenaline APIs or Orciprenaline finished pharmaceutical products to another nation, regulatory agencies frequently require a Orciprenaline WC (written confirmation) as part of the regulatory process.
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