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ABOUT THIS PAGE
A Tetramisole Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetramisole Hydrochloride, including repackagers and relabelers. The FDA regulates Tetramisole Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetramisole 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 Tetramisole Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tetramisole Hydrochloride supplier is an individual or a company that provides Tetramisole Hydrochloride active pharmaceutical ingredient (API) or Tetramisole Hydrochloride finished formulations upon request. The Tetramisole Hydrochloride suppliers may include Tetramisole Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Tetramisole Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tetramisole Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Tetramisole Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Tetramisole Hydrochloride DMFs exist exist since differing nations have different regulations, such as Tetramisole Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tetramisole Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Tetramisole Hydrochloride USDMF includes data on Tetramisole Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tetramisole Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tetramisole Hydrochloride suppliers with USDMF on PharmaCompass.
Tetramisole 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 Tetramisole 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 Tetramisole Hydrochloride GMP manufacturer or Tetramisole Hydrochloride GMP API supplier for your needs.
A Tetramisole Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Tetramisole Hydrochloride's compliance with Tetramisole Hydrochloride specifications and serves as a tool for batch-level quality control.
Tetramisole Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Tetramisole 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.
Tetramisole Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Tetramisole Hydrochloride EP), Tetramisole Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tetramisole Hydrochloride USP).
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