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API SUPPLIERS
Veranova: A CDMO that manages complexity with confidence.
KDMF
ROW 
Temad- We think of world-class quality.
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Aspen API. More than just an API™
Veranova: A CDMO that manages complexity with confidence.
ROW
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Pfanstiehl
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ABOUT THIS PAGE
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PharmaCompass offers a list of Morphine Hydrochloride 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 Morphine Hydrochloride manufacturer or Morphine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Morphine Hydrochloride manufacturer or Morphine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Morphine Hydrochloride API Price utilized in the formulation of products. Morphine Hydrochloride API Price is not always fixed or binding as the Morphine Hydrochloride Price is obtained through a variety of data sources. The Morphine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Epimore manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Epimore, including repackagers and relabelers. The FDA regulates Epimore manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Epimore 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 Epimore manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Epimore supplier is an individual or a company that provides Epimore active pharmaceutical ingredient (API) or Epimore finished formulations upon request. The Epimore suppliers may include Epimore API manufacturers, exporters, distributors and traders.
click here to find a list of Epimore suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Epimore Drug Master File in Japan (Epimore JDMF) empowers Epimore API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Epimore JDMF during the approval evaluation for pharmaceutical products. At the time of Epimore JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Epimore suppliers with JDMF 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 Epimore Drug Master File in Korea (Epimore KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Epimore. The MFDS reviews the Epimore KDMF as part of the drug registration process and uses the information provided in the Epimore KDMF to evaluate the safety and efficacy of the drug.
After submitting a Epimore 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 Epimore API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Epimore suppliers with KDMF on PharmaCompass.
A Epimore CEP of the European Pharmacopoeia monograph is often referred to as a Epimore Certificate of Suitability (COS). The purpose of a Epimore CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Epimore EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Epimore to their clients by showing that a Epimore CEP has been issued for it. The manufacturer submits a Epimore CEP (COS) as part of the market authorization procedure, and it takes on the role of a Epimore CEP holder for the record. Additionally, the data presented in the Epimore CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Epimore DMF.
A Epimore CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Epimore 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 Epimore suppliers with CEP (COS) on PharmaCompass.
Epimore 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 Epimore 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 Epimore GMP manufacturer or Epimore GMP API supplier for your needs.
A Epimore CoA (Certificate of Analysis) is a formal document that attests to Epimore's compliance with Epimore specifications and serves as a tool for batch-level quality control.
Epimore CoA mostly includes findings from lab analyses of a specific batch. For each Epimore 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.
Epimore may be tested according to a variety of international standards, such as European Pharmacopoeia (Epimore EP), Epimore JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Epimore USP).
