Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1M/s Symbiotec Pharmalab Private Limited
02 1M/s Symbiotec Pharmalab Private limited
03 1M/s Symbiotec Pharmalab Pvt Ltd
04 1Hubei Gedian Humanwell Pharmaceutical Co., Ltd
05 1M/s La Chandra Pharmalab Pvt Ltd
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Date of Issue : 2022-06-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161A2
Address of the Firm : 385/2, Gram Pigdamber, Rau, Indore-453331, M.P., 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-0162Amended
Address of the Firm : Plot No. 5,6,7 & 8, Special Economic Zone, Phase II, Pharma Zone, Pithampur, Dis...
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Date of Issue : 2022-07-23
Valid Till : 2025-02-07
Written Confirmation Number : WC-0162n
Address of the Firm : Plot No-5,6,7 & 8, Special Economic Zone, Phase-II, Pharma Zone, Pithampur, Dist...
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A CIDR manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CIDR, including repackagers and relabelers. The FDA regulates CIDR manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CIDR API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of CIDR manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A CIDR supplier is an individual or a company that provides CIDR active pharmaceutical ingredient (API) or CIDR finished formulations upon request. The CIDR suppliers may include CIDR API manufacturers, exporters, distributors and traders.
click here to find a list of CIDR suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A CIDR written confirmation (CIDR WC) is an official document issued by a regulatory agency to a CIDR manufacturer, verifying that the manufacturing facility of a CIDR active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting CIDR APIs or CIDR finished pharmaceutical products to another nation, regulatory agencies frequently require a CIDR WC (written confirmation) as part of the regulatory process.
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