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API SUPPLIERS
Lifecare Labs has been developing innovative products in specialist areas of medicine.
JDMF
EU-WC
Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
Jai Radhe Sales is your partner for all your sourcing needs.
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
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CEP/COS
Lifecare Labs has been developing innovative products in specialist areas of medicine.
Certificate Number : R0-CEP 2018-226 - Rev 00
Status : Valid
Issue Date : 2021-10-26
Type : Chemical
Substance Number : 1074
Certificate Number : R2-CEP 1995-038 - Rev 05
Status : Valid
Issue Date : 2019-01-24
Type : Chemical
Substance Number : 1074
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Lifecare Labs has been developing innovative products in specialist areas of medicine.
Registration Number : 305MF10051
Registrant's Address : 78/A, Bengalrao Nagar, Hyderabad-500 038, Telangana State, India.
Initial Date of Registration : 2023-04-25
Latest Date of Registration : 2023-04-25
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Lifecare Labs has been developing innovative products in specialist areas of medicine.
Biperiden Hydrochloride Ph. Eur
Date of Issue : 2023-06-01
Valid Till : 2025-10-14
Written Confirmation Number : WC-0456
Address of the Firm : #102, Doyen Chambers, Behind Saradhi Studio, Ameerpet, Hyderabad - 500 073, Tela...
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PharmaCompass offers a list of Biperiden 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 Biperiden Hydrochloride manufacturer or Biperiden Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Biperiden Hydrochloride manufacturer or Biperiden Hydrochloride supplier.
PharmaCompass also assists you with knowing the Biperiden Hydrochloride API Price utilized in the formulation of products. Biperiden Hydrochloride API Price is not always fixed or binding as the Biperiden Hydrochloride Price is obtained through a variety of data sources. The Biperiden Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Biperiden Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Biperiden Hydrochloride, including repackagers and relabelers. The FDA regulates Biperiden Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Biperiden 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 Biperiden Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Biperiden Hydrochloride supplier is an individual or a company that provides Biperiden Hydrochloride active pharmaceutical ingredient (API) or Biperiden Hydrochloride finished formulations upon request. The Biperiden Hydrochloride suppliers may include Biperiden Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Biperiden 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 Biperiden Hydrochloride Drug Master File in Japan (Biperiden Hydrochloride JDMF) empowers Biperiden 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 Biperiden Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Biperiden 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 Biperiden Hydrochloride suppliers with JDMF on PharmaCompass.
A Biperiden Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Biperiden Hydrochloride Certificate of Suitability (COS). The purpose of a Biperiden Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Biperiden Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Biperiden Hydrochloride to their clients by showing that a Biperiden Hydrochloride CEP has been issued for it. The manufacturer submits a Biperiden Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Biperiden Hydrochloride CEP holder for the record. Additionally, the data presented in the Biperiden Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Biperiden Hydrochloride DMF.
A Biperiden Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Biperiden Hydrochloride 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 Biperiden Hydrochloride suppliers with CEP (COS) on PharmaCompass.
A Biperiden Hydrochloride written confirmation (Biperiden Hydrochloride WC) is an official document issued by a regulatory agency to a Biperiden Hydrochloride manufacturer, verifying that the manufacturing facility of a Biperiden Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Biperiden Hydrochloride APIs or Biperiden Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Biperiden Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Biperiden Hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
Biperiden 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 Biperiden 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 Biperiden Hydrochloride GMP manufacturer or Biperiden Hydrochloride GMP API supplier for your needs.
A Biperiden Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Biperiden Hydrochloride's compliance with Biperiden Hydrochloride specifications and serves as a tool for batch-level quality control.
Biperiden Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Biperiden 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.
Biperiden Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Biperiden Hydrochloride EP), Biperiden Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Biperiden Hydrochloride USP).
