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ABOUT THIS PAGE
A Pilsicainide Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pilsicainide Hydrochloride, including repackagers and relabelers. The FDA regulates Pilsicainide Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pilsicainide Hydrochloride 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 Pilsicainide Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pilsicainide Hydrochloride supplier is an individual or a company that provides Pilsicainide Hydrochloride active pharmaceutical ingredient (API) or Pilsicainide Hydrochloride finished formulations upon request. The Pilsicainide Hydrochloride suppliers may include Pilsicainide Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Pilsicainide Hydrochloride 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 Pilsicainide Hydrochloride Drug Master File in Japan (Pilsicainide Hydrochloride JDMF) empowers Pilsicainide Hydrochloride 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 Pilsicainide Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Pilsicainide Hydrochloride 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 Pilsicainide Hydrochloride 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 Pilsicainide Hydrochloride Drug Master File in Korea (Pilsicainide Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Pilsicainide Hydrochloride. The MFDS reviews the Pilsicainide Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Pilsicainide Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Pilsicainide Hydrochloride 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 Pilsicainide Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Pilsicainide Hydrochloride suppliers with KDMF on PharmaCompass.
Pilsicainide Hydrochloride 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 Pilsicainide Hydrochloride 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 Pilsicainide Hydrochloride GMP manufacturer or Pilsicainide Hydrochloride GMP API supplier for your needs.
A Pilsicainide Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Pilsicainide Hydrochloride's compliance with Pilsicainide Hydrochloride specifications and serves as a tool for batch-level quality control.
Pilsicainide Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Pilsicainide Hydrochloride 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.
Pilsicainide Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Pilsicainide Hydrochloride EP), Pilsicainide Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Pilsicainide Hydrochloride USP).
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