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PharmaCompass offers a list of Teriparatide Acetate 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 Teriparatide Acetate manufacturer or Teriparatide Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Teriparatide Acetate manufacturer or Teriparatide Acetate supplier.
PharmaCompass also assists you with knowing the Teriparatide Acetate API Price utilized in the formulation of products. Teriparatide Acetate API Price is not always fixed or binding as the Teriparatide Acetate Price is obtained through a variety of data sources. The Teriparatide Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Parathar Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Parathar Acetate, including repackagers and relabelers. The FDA regulates Parathar Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Parathar Acetate 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 Parathar Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Parathar Acetate supplier is an individual or a company that provides Parathar Acetate active pharmaceutical ingredient (API) or Parathar Acetate finished formulations upon request. The Parathar Acetate suppliers may include Parathar Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Parathar Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Parathar Acetate DMF (Drug Master File) is a document detailing the whole manufacturing process of Parathar Acetate active pharmaceutical ingredient (API) in detail. Different forms of Parathar Acetate DMFs exist exist since differing nations have different regulations, such as Parathar Acetate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Parathar Acetate DMF submitted to regulatory agencies in the US is known as a USDMF. Parathar Acetate USDMF includes data on Parathar Acetate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Parathar Acetate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Parathar Acetate 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 Parathar Acetate Drug Master File in Japan (Parathar Acetate JDMF) empowers Parathar Acetate 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 Parathar Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Parathar Acetate 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 Parathar Acetate 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 Parathar Acetate Drug Master File in Korea (Parathar Acetate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Parathar Acetate. The MFDS reviews the Parathar Acetate KDMF as part of the drug registration process and uses the information provided in the Parathar Acetate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Parathar Acetate 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 Parathar Acetate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Parathar Acetate suppliers with KDMF on PharmaCompass.
A Parathar Acetate written confirmation (Parathar Acetate WC) is an official document issued by a regulatory agency to a Parathar Acetate manufacturer, verifying that the manufacturing facility of a Parathar Acetate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Parathar Acetate APIs or Parathar Acetate finished pharmaceutical products to another nation, regulatory agencies frequently require a Parathar Acetate WC (written confirmation) as part of the regulatory process.
click here to find a list of Parathar Acetate suppliers with Written Confirmation (WC) 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 Parathar Acetate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Parathar Acetate 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 Parathar Acetate 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 Parathar Acetate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Parathar Acetate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Parathar Acetate suppliers with NDC on PharmaCompass.
Parathar Acetate 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 Parathar Acetate 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 Parathar Acetate GMP manufacturer or Parathar Acetate GMP API supplier for your needs.
A Parathar Acetate CoA (Certificate of Analysis) is a formal document that attests to Parathar Acetate's compliance with Parathar Acetate specifications and serves as a tool for batch-level quality control.
Parathar Acetate CoA mostly includes findings from lab analyses of a specific batch. For each Parathar Acetate 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.
Parathar Acetate may be tested according to a variety of international standards, such as European Pharmacopoeia (Parathar Acetate EP), Parathar Acetate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Parathar Acetate USP).
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