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Looking for 67-66-3 / Chloroform API manufacturers, exporters & distributors?

Chloroform manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Chloroform 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 Chloroform manufacturer or Chloroform supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chloroform manufacturer or Chloroform supplier.

PharmaCompass also assists you with knowing the Chloroform API Price utilized in the formulation of products. Chloroform API Price is not always fixed or binding as the Chloroform Price is obtained through a variety of data sources. The Chloroform Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Chloroform

Synonyms

Trichloromethane, 67-66-3, Methane, trichloro-, Trichlormethan, Formyl trichloride, Trichloroform

Cas Number

67-66-3

Unique Ingredient Identifier (UNII)

7V31YC746X

About Chloroform

A commonly used laboratory solvent. It was previously used as an anesthetic, but was banned from use in the U.S. due to its suspected carcinogenicity.

02487_FLUKA Manufacturers

A 02487_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 02487_FLUKA, including repackagers and relabelers. The FDA regulates 02487_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 02487_FLUKA API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

02487_FLUKA Suppliers

A 02487_FLUKA supplier is an individual or a company that provides 02487_FLUKA active pharmaceutical ingredient (API) or 02487_FLUKA finished formulations upon request. The 02487_FLUKA suppliers may include 02487_FLUKA API manufacturers, exporters, distributors and traders.

click here to find a list of 02487_FLUKA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

02487_FLUKA USDMF

A 02487_FLUKA DMF (Drug Master File) is a document detailing the whole manufacturing process of 02487_FLUKA active pharmaceutical ingredient (API) in detail. Different forms of 02487_FLUKA DMFs exist exist since differing nations have different regulations, such as 02487_FLUKA USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 02487_FLUKA DMF submitted to regulatory agencies in the US is known as a USDMF. 02487_FLUKA USDMF includes data on 02487_FLUKA's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 02487_FLUKA USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 02487_FLUKA suppliers with USDMF on PharmaCompass.

02487_FLUKA GMP

02487_FLUKA 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 02487_FLUKA 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 02487_FLUKA GMP manufacturer or 02487_FLUKA GMP API supplier for your needs.

02487_FLUKA CoA

A 02487_FLUKA CoA (Certificate of Analysis) is a formal document that attests to 02487_FLUKA's compliance with 02487_FLUKA specifications and serves as a tool for batch-level quality control.

02487_FLUKA CoA mostly includes findings from lab analyses of a specific batch. For each 02487_FLUKA 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.

02487_FLUKA may be tested according to a variety of international standards, such as European Pharmacopoeia (02487_FLUKA EP), 02487_FLUKA JP (Japanese Pharmacopeia) and the US Pharmacopoeia (02487_FLUKA USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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