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Looking for 14392-02-0 / Chromium-51 API manufacturers, exporters & distributors?

Chromium-51 manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Chromium-51 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 Chromium-51 manufacturer or Chromium-51 supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chromium-51 manufacturer or Chromium-51 supplier.

PharmaCompass also assists you with knowing the Chromium-51 API Price utilized in the formulation of products. Chromium-51 API Price is not always fixed or binding as the Chromium-51 Price is obtained through a variety of data sources. The Chromium-51 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Chromium-51

Synonyms

Chromium cr-51, Chromium cr 51, 14392-02-0, 51cr, Chromium, isotope of mass 51, Chromium (51 cr)

Cas Number

14392-02-0

Unique Ingredient Identifier (UNII)

9QAU17N705

About Chromium-51

Chromium Cr-51 is an isotope of chromium that is observationally stable. When intravenously administered, it is used as a diagnostic radiopharmaceutical agent to determine the red blood cell volume or mass, study the red blood cell survival time and evaluate blood loss.

CHROMIUM 51 Manufacturers

A CHROMIUM 51 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CHROMIUM 51, including repackagers and relabelers. The FDA regulates CHROMIUM 51 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CHROMIUM 51 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

CHROMIUM 51 Suppliers

A CHROMIUM 51 supplier is an individual or a company that provides CHROMIUM 51 active pharmaceutical ingredient (API) or CHROMIUM 51 finished formulations upon request. The CHROMIUM 51 suppliers may include CHROMIUM 51 API manufacturers, exporters, distributors and traders.

click here to find a list of CHROMIUM 51 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

CHROMIUM 51 USDMF

A CHROMIUM 51 DMF (Drug Master File) is a document detailing the whole manufacturing process of CHROMIUM 51 active pharmaceutical ingredient (API) in detail. Different forms of CHROMIUM 51 DMFs exist exist since differing nations have different regulations, such as CHROMIUM 51 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A CHROMIUM 51 DMF submitted to regulatory agencies in the US is known as a USDMF. CHROMIUM 51 USDMF includes data on CHROMIUM 51's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The CHROMIUM 51 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of CHROMIUM 51 suppliers with USDMF on PharmaCompass.

CHROMIUM 51 GMP

CHROMIUM 51 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 CHROMIUM 51 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 CHROMIUM 51 GMP manufacturer or CHROMIUM 51 GMP API supplier for your needs.

CHROMIUM 51 CoA

A CHROMIUM 51 CoA (Certificate of Analysis) is a formal document that attests to CHROMIUM 51's compliance with CHROMIUM 51 specifications and serves as a tool for batch-level quality control.

CHROMIUM 51 CoA mostly includes findings from lab analyses of a specific batch. For each CHROMIUM 51 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.

CHROMIUM 51 may be tested according to a variety of international standards, such as European Pharmacopoeia (CHROMIUM 51 EP), CHROMIUM 51 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (CHROMIUM 51 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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