Synopsis
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
NDC API
0
VMF
0
EDQM
0
USP
0
JP
0
Others
0
FDA Orange Book
0
Canada
0
Australia
0
South Africa
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
Listed Suppliers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Global Sales Information
Market Place
ABOUT THIS PAGE
10
PharmaCompass offers a list of Acetyl-L-Carnitine 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 Acetyl-L-Carnitine Hydrochloride manufacturer or Acetyl-L-Carnitine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Acetyl-L-Carnitine Hydrochloride manufacturer or Acetyl-L-Carnitine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Acetyl-L-Carnitine Hydrochloride API Price utilized in the formulation of products. Acetyl-L-Carnitine Hydrochloride API Price is not always fixed or binding as the Acetyl-L-Carnitine Hydrochloride Price is obtained through a variety of data sources. The Acetyl-L-Carnitine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nicetile manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nicetile, including repackagers and relabelers. The FDA regulates Nicetile manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nicetile 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 Nicetile manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nicetile supplier is an individual or a company that provides Nicetile active pharmaceutical ingredient (API) or Nicetile finished formulations upon request. The Nicetile suppliers may include Nicetile API manufacturers, exporters, distributors and traders.
click here to find a list of Nicetile suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Nicetile Drug Master File in Korea (Nicetile KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Nicetile. The MFDS reviews the Nicetile KDMF as part of the drug registration process and uses the information provided in the Nicetile KDMF to evaluate the safety and efficacy of the drug.
After submitting a Nicetile 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 Nicetile API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Nicetile suppliers with KDMF on PharmaCompass.
Nicetile 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 Nicetile 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 Nicetile GMP manufacturer or Nicetile GMP API supplier for your needs.
A Nicetile CoA (Certificate of Analysis) is a formal document that attests to Nicetile's compliance with Nicetile specifications and serves as a tool for batch-level quality control.
Nicetile CoA mostly includes findings from lab analyses of a specific batch. For each Nicetile 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.
Nicetile may be tested according to a variety of international standards, such as European Pharmacopoeia (Nicetile EP), Nicetile JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Nicetile USP).
