Synopsis
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NDC API
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FDA Orange Book
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Europe
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Data Compilation #PharmaFlow
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API SUPPLIERS
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
ASMF 
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CEP/COS
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : R1-CEP 2003-181 - Rev 01
Status : Valid
Issue Date : 2017-01-05
Type : Chemical
Substance Number : 1980
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Certificate Number : R1-CEP 2001-154 - Rev 05
Status : Valid
Issue Date : 2021-08-06
Type : Chemical
Substance Number : 1980
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Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
About the Company : Since its inception in 2003, Seqens has evolved into a global leader in pharmaceutical solutions and specialty ingredients. With a strong focus on customer support, Seqens assists ...
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APIs
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21 Sep 2019
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16 Aug 2019
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Heptaminol 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 Heptaminol manufacturer or Heptaminol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Heptaminol manufacturer or Heptaminol supplier.
PharmaCompass also assists you with knowing the Heptaminol API Price utilized in the formulation of products. Heptaminol API Price is not always fixed or binding as the Heptaminol Price is obtained through a variety of data sources. The Heptaminol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Heptamyl hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Heptamyl hydrochloride, including repackagers and relabelers. The FDA regulates Heptamyl hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Heptamyl 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 Heptamyl hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Heptamyl hydrochloride supplier is an individual or a company that provides Heptamyl hydrochloride active pharmaceutical ingredient (API) or Heptamyl hydrochloride finished formulations upon request. The Heptamyl hydrochloride suppliers may include Heptamyl hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Heptamyl hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Heptamyl hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Heptamyl hydrochloride Certificate of Suitability (COS). The purpose of a Heptamyl hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Heptamyl hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Heptamyl hydrochloride to their clients by showing that a Heptamyl hydrochloride CEP has been issued for it. The manufacturer submits a Heptamyl hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Heptamyl hydrochloride CEP holder for the record. Additionally, the data presented in the Heptamyl hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Heptamyl hydrochloride DMF.
A Heptamyl hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Heptamyl hydrochloride 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 Heptamyl hydrochloride suppliers with CEP (COS) on PharmaCompass.
Heptamyl 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 Heptamyl 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 Heptamyl hydrochloride GMP manufacturer or Heptamyl hydrochloride GMP API supplier for your needs.
A Heptamyl hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Heptamyl hydrochloride's compliance with Heptamyl hydrochloride specifications and serves as a tool for batch-level quality control.
Heptamyl hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Heptamyl 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.
Heptamyl hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Heptamyl hydrochloride EP), Heptamyl hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Heptamyl hydrochloride USP).
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