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PharmaCompass offers a list of Calcium Pantothenate 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 Calcium Pantothenate manufacturer or Calcium Pantothenate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcium Pantothenate manufacturer or Calcium Pantothenate supplier.
PharmaCompass also assists you with knowing the Calcium Pantothenate API Price utilized in the formulation of products. Calcium Pantothenate API Price is not always fixed or binding as the Calcium Pantothenate Price is obtained through a variety of data sources. The Calcium Pantothenate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Calcium D-Pantothenate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Calcium D-Pantothenate, including repackagers and relabelers. The FDA regulates Calcium D-Pantothenate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Calcium D-Pantothenate 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 Calcium D-Pantothenate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Calcium D-Pantothenate supplier is an individual or a company that provides Calcium D-Pantothenate active pharmaceutical ingredient (API) or Calcium D-Pantothenate finished formulations upon request. The Calcium D-Pantothenate suppliers may include Calcium D-Pantothenate API manufacturers, exporters, distributors and traders.
click here to find a list of Calcium D-Pantothenate 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 Calcium D-Pantothenate Drug Master File in Japan (Calcium D-Pantothenate JDMF) empowers Calcium D-Pantothenate 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 Calcium D-Pantothenate JDMF during the approval evaluation for pharmaceutical products. At the time of Calcium D-Pantothenate 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 Calcium D-Pantothenate 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 Calcium D-Pantothenate Drug Master File in Korea (Calcium D-Pantothenate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Calcium D-Pantothenate. The MFDS reviews the Calcium D-Pantothenate KDMF as part of the drug registration process and uses the information provided in the Calcium D-Pantothenate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Calcium D-Pantothenate 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 Calcium D-Pantothenate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Calcium D-Pantothenate suppliers with KDMF on PharmaCompass.
Calcium D-Pantothenate 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 Calcium D-Pantothenate 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 Calcium D-Pantothenate GMP manufacturer or Calcium D-Pantothenate GMP API supplier for your needs.
A Calcium D-Pantothenate CoA (Certificate of Analysis) is a formal document that attests to Calcium D-Pantothenate's compliance with Calcium D-Pantothenate specifications and serves as a tool for batch-level quality control.
Calcium D-Pantothenate CoA mostly includes findings from lab analyses of a specific batch. For each Calcium D-Pantothenate 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.
Calcium D-Pantothenate may be tested according to a variety of international standards, such as European Pharmacopoeia (Calcium D-Pantothenate EP), Calcium D-Pantothenate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Calcium D-Pantothenate USP).
