Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
01 1M/s Aarti Pharmalabs limited
02 1M/s.Srini Pharmaceuticals Private Limited
01 1Deferiprone IH/Ph. Eur
02 1Deferiprone Ph. Eur
01 1WC-0295
02 1WC-0313
01 2India
Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
Date of Issue : 2024-05-20
Valid Till : 2027-05-19
Written Confirmation Number : WC-0295
Address of the Firm : D-53, PHASE II, KALYAN SHILL ROAD, DOMBIVLI (E.), DOMBIVLI - 421204, Taluka: Dom...
Date of Issue : 2023-07-10
Valid Till : 2025-05-21
Written Confirmation Number : WC-0313
Address of the Firm : SurveyNo.247,Choutuppal, Choutuppal (V),Choutuppal (M),YadadriBhuvanagiri Distri...
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A CRMD-001 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CRMD-001, including repackagers and relabelers. The FDA regulates CRMD-001 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CRMD-001 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 CRMD-001 supplier is an individual or a company that provides CRMD-001 active pharmaceutical ingredient (API) or CRMD-001 finished formulations upon request. The CRMD-001 suppliers may include CRMD-001 API manufacturers, exporters, distributors and traders.
click here to find a list of CRMD-001 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CRMD-001 written confirmation (CRMD-001 WC) is an official document issued by a regulatory agency to a CRMD-001 manufacturer, verifying that the manufacturing facility of a CRMD-001 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting CRMD-001 APIs or CRMD-001 finished pharmaceutical products to another nation, regulatory agencies frequently require a CRMD-001 WC (written confirmation) as part of the regulatory process.
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