Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1M/s. Symbiotec Pharmalab Ltd
01 1Prednisolone BP/EP/USP
01 1WC-0162A2
01 1India
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Date of Issue : 2022-08-31
Valid Till : 2025-07-02
Written Confirmation Number : WC-0162A2
Address of the Firm : Plot No. 5, 6, 7 & 8 Special Economic Zone, Phase II, Pithampur, Dist: Dhar, MP-...
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PharmaCompass also assists you with knowing the Prednisolone API Price utilized in the formulation of products. Prednisolone API Price is not always fixed or binding as the Prednisolone Price is obtained through a variety of data sources. The Prednisolone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hydeltra-TBA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydeltra-TBA, including repackagers and relabelers. The FDA regulates Hydeltra-TBA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydeltra-TBA 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 Hydeltra-TBA supplier is an individual or a company that provides Hydeltra-TBA active pharmaceutical ingredient (API) or Hydeltra-TBA finished formulations upon request. The Hydeltra-TBA suppliers may include Hydeltra-TBA API manufacturers, exporters, distributors and traders.
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A Hydeltra-TBA written confirmation (Hydeltra-TBA WC) is an official document issued by a regulatory agency to a Hydeltra-TBA manufacturer, verifying that the manufacturing facility of a Hydeltra-TBA active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Hydeltra-TBA APIs or Hydeltra-TBA finished pharmaceutical products to another nation, regulatory agencies frequently require a Hydeltra-TBA WC (written confirmation) as part of the regulatory process.
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