API Suppliers
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PharmaCompass offers a list of Somatostatin 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 Somatostatin manufacturer or Somatostatin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Somatostatin manufacturer or Somatostatin supplier.
PharmaCompass also assists you with knowing the Somatostatin API Price utilized in the formulation of products. Somatostatin API Price is not always fixed or binding as the Somatostatin Price is obtained through a variety of data sources. The Somatostatin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Somatostatin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Somatostatin, including repackagers and relabelers. The FDA regulates Somatostatin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Somatostatin 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 Somatostatin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Somatostatin supplier is an individual or a company that provides Somatostatin active pharmaceutical ingredient (API) or Somatostatin finished formulations upon request. The Somatostatin suppliers may include Somatostatin API manufacturers, exporters, distributors and traders.
click here to find a list of Somatostatin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Somatostatin DMF (Drug Master File) is a document detailing the whole manufacturing process of Somatostatin active pharmaceutical ingredient (API) in detail. Different forms of Somatostatin DMFs exist exist since differing nations have different regulations, such as Somatostatin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Somatostatin DMF submitted to regulatory agencies in the US is known as a USDMF. Somatostatin USDMF includes data on Somatostatin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Somatostatin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Somatostatin suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Somatostatin Drug Master File in Korea (Somatostatin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Somatostatin. The MFDS reviews the Somatostatin KDMF as part of the drug registration process and uses the information provided in the Somatostatin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Somatostatin KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Somatostatin API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Somatostatin suppliers with KDMF on PharmaCompass.
A Somatostatin CEP of the European Pharmacopoeia monograph is often referred to as a Somatostatin Certificate of Suitability (COS). The purpose of a Somatostatin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Somatostatin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Somatostatin to their clients by showing that a Somatostatin CEP has been issued for it. The manufacturer submits a Somatostatin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Somatostatin CEP holder for the record. Additionally, the data presented in the Somatostatin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Somatostatin DMF.
A Somatostatin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Somatostatin CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Somatostatin suppliers with CEP (COS) on PharmaCompass.
A Somatostatin written confirmation (Somatostatin WC) is an official document issued by a regulatory agency to a Somatostatin manufacturer, verifying that the manufacturing facility of a Somatostatin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Somatostatin APIs or Somatostatin finished pharmaceutical products to another nation, regulatory agencies frequently require a Somatostatin WC (written confirmation) as part of the regulatory process.
click here to find a list of Somatostatin suppliers with Written Confirmation (WC) on PharmaCompass.
Somatostatin 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 Somatostatin 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 Somatostatin GMP manufacturer or Somatostatin GMP API supplier for your needs.
A Somatostatin CoA (Certificate of Analysis) is a formal document that attests to Somatostatin's compliance with Somatostatin specifications and serves as a tool for batch-level quality control.
Somatostatin CoA mostly includes findings from lab analyses of a specific batch. For each Somatostatin 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.
Somatostatin may be tested according to a variety of international standards, such as European Pharmacopoeia (Somatostatin EP), Somatostatin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Somatostatin USP).