Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1M/S Symbiotec Pharmalab
02 2M/s. Symbiotec Pharmalab Ltd
03 1Hubei Gedian Humanwell Pharmaceutical Co., Ltd
04 1M/s Naari Pharma Private Limited
05 1M/s. Indo Phyto Chemicals Pvt. Ltd.
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Date of Issue : 2022-09-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0162A2
Address of the Firm : 385/2, Pigdamber, Rau, Indore-453 331, MP, India
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-...
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Date of Issue : 2022-07-05
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161A2
Address of the Firm : 385/2, Pigdamber, Rau, Indore-453 331, MP, India
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PharmaCompass offers a list of Levonorgestrel API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Levonorgestrel manufacturer or Levonorgestrel supplier for your needs.
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A Neogynon 21 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neogynon 21, including repackagers and relabelers. The FDA regulates Neogynon 21 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neogynon 21 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 Neogynon 21 supplier is an individual or a company that provides Neogynon 21 active pharmaceutical ingredient (API) or Neogynon 21 finished formulations upon request. The Neogynon 21 suppliers may include Neogynon 21 API manufacturers, exporters, distributors and traders.
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A Neogynon 21 written confirmation (Neogynon 21 WC) is an official document issued by a regulatory agency to a Neogynon 21 manufacturer, verifying that the manufacturing facility of a Neogynon 21 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Neogynon 21 APIs or Neogynon 21 finished pharmaceutical products to another nation, regulatory agencies frequently require a Neogynon 21 WC (written confirmation) as part of the regulatory process.
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