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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 Morphine HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Morphine HCl, including repackagers and relabelers. The FDA regulates Morphine HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Morphine HCl 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 Morphine HCl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Morphine HCl supplier is an individual or a company that provides Morphine HCl active pharmaceutical ingredient (API) or Morphine HCl finished formulations upon request. The Morphine HCl suppliers may include Morphine HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Morphine HCl 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 Morphine HCl Drug Master File in Japan (Morphine HCl JDMF) empowers Morphine HCl 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 Morphine HCl JDMF during the approval evaluation for pharmaceutical products. At the time of Morphine HCl 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 Morphine HCl 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 Morphine HCl Drug Master File in Korea (Morphine HCl KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Morphine HCl. The MFDS reviews the Morphine HCl KDMF as part of the drug registration process and uses the information provided in the Morphine HCl KDMF to evaluate the safety and efficacy of the drug.
After submitting a Morphine HCl 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 Morphine HCl API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Morphine HCl suppliers with KDMF on PharmaCompass.
A Morphine HCl CEP of the European Pharmacopoeia monograph is often referred to as a Morphine HCl Certificate of Suitability (COS). The purpose of a Morphine HCl CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Morphine HCl EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Morphine HCl to their clients by showing that a Morphine HCl CEP has been issued for it. The manufacturer submits a Morphine HCl CEP (COS) as part of the market authorization procedure, and it takes on the role of a Morphine HCl CEP holder for the record. Additionally, the data presented in the Morphine HCl CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Morphine HCl DMF.
A Morphine HCl CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Morphine HCl 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 Morphine HCl suppliers with CEP (COS) on PharmaCompass.
Morphine HCl 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 Morphine HCl 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 Morphine HCl GMP manufacturer or Morphine HCl GMP API supplier for your needs.
A Morphine HCl CoA (Certificate of Analysis) is a formal document that attests to Morphine HCl's compliance with Morphine HCl specifications and serves as a tool for batch-level quality control.
Morphine HCl CoA mostly includes findings from lab analyses of a specific batch. For each Morphine HCl 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.
Morphine HCl may be tested according to a variety of international standards, such as European Pharmacopoeia (Morphine HCl EP), Morphine HCl JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Morphine HCl USP).
