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Looking for 1257628-77-5 / Olverembatinib API manufacturers, exporters & distributors?

Olverembatinib manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Olverembatinib

Synonyms

1257628-77-5, Gzd824, Gzd-824, Hqp1351, Olverembatinib [usan], Hqp-1351

Cas Number

1257628-77-5

Unique Ingredient Identifier (UNII)

KV1M7Q3CBP

About Olverembatinib

Olverembatinib is an orally bioavailable inhibitor of a variety of kinases, including the Bcr-Abl tyrosine kinase, the mast/stem cell growth factor receptor Kit (c-Kit), the serine/threonine protein kinase Akt (protein kinase B), and the extracellular signal-regulated kinase (ERK) with antineoplastic activity. Upon administration,olverembatinib targets, binds to and inhibits the kinase activities of Bcr-Abl, AKT, c-Kit and ERK. This inhibits their mediated signaling pathways and inhibits proliferation of tumor cells in which these kinases are overexpressed and/or mutated. Bcr-Abl, c-Kit, AKT and ERK play key roles in the proliferation, differentiation and survival of tumor cells.

Olverembatinib Manufacturers

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

Olverembatinib Suppliers

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

Olverembatinib GMP

Olverembatinib 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 Olverembatinib 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 Olverembatinib GMP manufacturer or Olverembatinib GMP API supplier for your needs.

Olverembatinib CoA

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

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

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