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API SUPPLIERS
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Listed Suppliers
Reliable Spanish CDMO Delivering High-Quality APIs and Intermediates with Excellence, Flexibility, and Regulatory Compliance.
About the Company : Kinsy, an independent CDMO in Spain, offers over 30 years of expertise in developing and manufacturing advanced pharmaceutical intermediates and APIs. We provide innovative route d...
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A Dembrexine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dembrexine Hydrochloride, including repackagers and relabelers. The FDA regulates Dembrexine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dembrexine Hydrochloride 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 Dembrexine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dembrexine Hydrochloride supplier is an individual or a company that provides Dembrexine Hydrochloride active pharmaceutical ingredient (API) or Dembrexine Hydrochloride finished formulations upon request. The Dembrexine Hydrochloride suppliers may include Dembrexine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Dembrexine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Dembrexine Hydrochloride Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Dembrexine Hydrochloride GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Dembrexine Hydrochloride GMP manufacturer or Dembrexine Hydrochloride GMP API supplier for your needs.
A Dembrexine Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Dembrexine Hydrochloride's compliance with Dembrexine Hydrochloride specifications and serves as a tool for batch-level quality control.
Dembrexine Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Dembrexine Hydrochloride CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Dembrexine Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Dembrexine Hydrochloride EP), Dembrexine Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dembrexine Hydrochloride USP).
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