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DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
About the Company : DKSH, founded with the goal of improving people's lives, assists businesses with market expansion and business growth in both existing and emerging markets. It has been fostering g...
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PharmaCompass offers a list of Procaine 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 Procaine manufacturer or Procaine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Procaine manufacturer or Procaine supplier.
PharmaCompass also assists you with knowing the Procaine API Price utilized in the formulation of products. Procaine API Price is not always fixed or binding as the Procaine Price is obtained through a variety of data sources. The Procaine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PROCAINE HCL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PROCAINE HCL, including repackagers and relabelers. The FDA regulates PROCAINE HCL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PROCAINE 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 PROCAINE HCL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PROCAINE HCL supplier is an individual or a company that provides PROCAINE HCL active pharmaceutical ingredient (API) or PROCAINE HCL finished formulations upon request. The PROCAINE HCL suppliers may include PROCAINE HCL API manufacturers, exporters, distributors and traders.
click here to find a list of PROCAINE HCL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A PROCAINE HCL DMF (Drug Master File) is a document detailing the whole manufacturing process of PROCAINE HCL active pharmaceutical ingredient (API) in detail. Different forms of PROCAINE HCL DMFs exist exist since differing nations have different regulations, such as PROCAINE HCL USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A PROCAINE HCL DMF submitted to regulatory agencies in the US is known as a USDMF. PROCAINE HCL USDMF includes data on PROCAINE HCL's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The PROCAINE HCL USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of PROCAINE HCL suppliers with USDMF 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 PROCAINE HCL Drug Master File in Japan (PROCAINE HCL JDMF) empowers PROCAINE 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 PROCAINE HCL JDMF during the approval evaluation for pharmaceutical products. At the time of PROCAINE 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 PROCAINE HCL suppliers with JDMF on PharmaCompass.
A PROCAINE HCL CEP of the European Pharmacopoeia monograph is often referred to as a PROCAINE HCL Certificate of Suitability (COS). The purpose of a PROCAINE HCL CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of PROCAINE HCL EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of PROCAINE HCL to their clients by showing that a PROCAINE HCL CEP has been issued for it. The manufacturer submits a PROCAINE HCL CEP (COS) as part of the market authorization procedure, and it takes on the role of a PROCAINE HCL CEP holder for the record. Additionally, the data presented in the PROCAINE HCL CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the PROCAINE HCL DMF.
A PROCAINE HCL CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. PROCAINE 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 PROCAINE HCL suppliers with CEP (COS) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing PROCAINE HCL as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for PROCAINE HCL API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture PROCAINE HCL as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain PROCAINE HCL and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a PROCAINE HCL NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of PROCAINE HCL suppliers with NDC on PharmaCompass.
PROCAINE 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 PROCAINE 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 PROCAINE HCL GMP manufacturer or PROCAINE HCL GMP API supplier for your needs.
A PROCAINE HCL CoA (Certificate of Analysis) is a formal document that attests to PROCAINE HCL's compliance with PROCAINE HCL specifications and serves as a tool for batch-level quality control.
PROCAINE HCL CoA mostly includes findings from lab analyses of a specific batch. For each PROCAINE 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.
PROCAINE HCL may be tested according to a variety of international standards, such as European Pharmacopoeia (PROCAINE HCL EP), PROCAINE HCL JP (Japanese Pharmacopeia) and the US Pharmacopoeia (PROCAINE HCL USP).
