USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
01 1USV PRIVATE LIMITED Mumbai IN
02 1ACTAVIS GROUP PTC EHF Hafnarfjordur IS
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1BIOCON LIMITED Bengaluru IN
05 1Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE
06 1CHROMO LABORATORIES INDIA PRIVATE LIMITED Pashamylaram IN
07 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
08 1JUBILANT PHARMOVA LIMITED Nanjangud IN
09 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
10 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
11 1Torrent Pharmaceuticals Limited Ahmedabad IN
12 1ZAKŁADY FARMACEUTYCZNE POLPHARMA S.A. Starogard Gdański PL
13 1ZHEJIANG HISOAR CHUANNAN PHARMACEUTICAL CO., LTD. Taizhou City CN
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
Certificate Number : R1-CEP 2009-239 - Rev 02
Status : Valid
Issue Date : 2019-02-22
Type : Chemical
Substance Number : 2135
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PharmaCompass offers a list of Repaglinide 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 Repaglinide manufacturer or Repaglinide supplier for your needs.
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PharmaCompass also assists you with knowing the Repaglinide API Price utilized in the formulation of products. Repaglinide API Price is not always fixed or binding as the Repaglinide Price is obtained through a variety of data sources. The Repaglinide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Repaglinide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Repaglinide, including repackagers and relabelers. The FDA regulates Repaglinide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Repaglinide 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 Repaglinide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Repaglinide supplier is an individual or a company that provides Repaglinide active pharmaceutical ingredient (API) or Repaglinide finished formulations upon request. The Repaglinide suppliers may include Repaglinide API manufacturers, exporters, distributors and traders.
click here to find a list of Repaglinide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Repaglinide CEP of the European Pharmacopoeia monograph is often referred to as a Repaglinide Certificate of Suitability (COS). The purpose of a Repaglinide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Repaglinide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Repaglinide to their clients by showing that a Repaglinide CEP has been issued for it. The manufacturer submits a Repaglinide CEP (COS) as part of the market authorization procedure, and it takes on the role of a Repaglinide CEP holder for the record. Additionally, the data presented in the Repaglinide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Repaglinide DMF.
A Repaglinide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Repaglinide 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 Repaglinide suppliers with CEP (COS) on PharmaCompass.
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