Reliable Spanish CDMO Delivering High-Quality APIs and Intermediates with Excellence, Flexibility, and Regulatory Compliance.
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01 1KINSY, S.L. Murcia ES
02 1EGIS Pharmaceuticals PLC Budapest HU
03 1Moehs Iberica S.L. Rubi ES
04 1Rusan Pharma Ltd. Mumbai IN
05 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
06 1AREVIPHARMA GMBH Radebeul DE
07 1BEIJING JINCHENG TAIER PHARMACEUTICAL CO., LTD. Beiwu Town CN
08 1CHENGDU EASTON BIOPHARMACEUTICALS CO., LTD. Chengdu CN
09 1CORDEN PHARMA CHENOVE CHENOVE FR
10 1EVONIK TECHNOCHEMIE GMBH Dossenheim DE
11 1HARMAN FINOCHEM LIMITED Mumbai IN
12 1IPCA LABORATORIES LIMITED Mumbai IN
13 1MEDILUX LABORATORIES PRIVATE LIMITED Pithampur IN
14 1MEHTA API PVT. LTD. Boisar IN
15 1MICRO LABS LIMITED Bengaluru IN
16 1Merck KGaA Darmstadt DE
17 1PIRAMAL PHARMA LIMITED Digwal Village IN
18 1TAIWAN BIOTECH CO., LTD. Taoyuan City TW
19 1Unichem Laboratories Limited Mumbai IN
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01 19Bisoprolol fumarate
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01 3China
02 4Germany
03 1Hungary
04 8India
05 2Spain
06 1U.S.A
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01 16Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 2Withdrawn by Holder
Reliable Spanish CDMO Delivering High-Quality APIs and Intermediates with Excellence, Flexibility, and Regulatory Compliance.
Reliable Spanish CDMO Delivering High-Quality APIs and Intermediates with Excellence, Flexibility, and Regulatory Compliance.
Certificate Number : R1-CEP 2015-243 - Rev 00
Status : Valid
Issue Date : 2022-02-03
Type : Chemical
Substance Number : 1710
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Certificate Number : R0-CEP 2019-090 - Rev 00
Status : Valid
Issue Date : 2021-03-16
Type : Chemical
Substance Number : 1710
Certificate Number : CEP 2009-044 - Rev 02
Status : Valid
Issue Date : 2024-08-16
Type : Chemical
Substance Number : 1710
Certificate Number : R0-CEP 2020-095 - Rev 00
Status : Valid
Issue Date : 2022-05-04
Type : Chemical
Substance Number : 1710
Certificate Number : CEP 2007-336 - Rev 04
Status : Valid
Issue Date : 2023-12-13
Type : Chemical
Substance Number : 1710
Certificate Number : R0-CEP 2018-209 - Rev 00
Status : Valid
Issue Date : 2020-09-11
Type : Chemical
Substance Number : 1710
Certificate Number : R1-CEP 2008-287 - Rev 01
Status : Valid
Issue Date : 2023-04-24
Type : Chemical
Substance Number : 1710
Certificate Number : CEP 2022-461 - Rev 00
Status : Valid
Issue Date : 2024-06-21
Type : Chemical
Substance Number : 1710
Certificate Number : CEP 2023-176 - Rev 00
Status : Valid
Issue Date : 2024-07-17
Type : Chemical
Substance Number : 1710
Certificate Number : CEP 2010-344 - Rev 02
Status : Valid
Issue Date : 2024-06-03
Type : Chemical
Substance Number : 1710
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PharmaCompass offers a list of Bisoprolol Fumarate 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 Bisoprolol Fumarate manufacturer or Bisoprolol Fumarate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bisoprolol Fumarate manufacturer or Bisoprolol Fumarate supplier.
PharmaCompass also assists you with knowing the Bisoprolol Fumarate API Price utilized in the formulation of products. Bisoprolol Fumarate API Price is not always fixed or binding as the Bisoprolol Fumarate Price is obtained through a variety of data sources. The Bisoprolol Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bisocard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bisocard, including repackagers and relabelers. The FDA regulates Bisocard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bisocard 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 Bisocard manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bisocard supplier is an individual or a company that provides Bisocard active pharmaceutical ingredient (API) or Bisocard finished formulations upon request. The Bisocard suppliers may include Bisocard API manufacturers, exporters, distributors and traders.
click here to find a list of Bisocard suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Bisocard CEP of the European Pharmacopoeia monograph is often referred to as a Bisocard Certificate of Suitability (COS). The purpose of a Bisocard CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Bisocard EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Bisocard to their clients by showing that a Bisocard CEP has been issued for it. The manufacturer submits a Bisocard CEP (COS) as part of the market authorization procedure, and it takes on the role of a Bisocard CEP holder for the record. Additionally, the data presented in the Bisocard CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Bisocard DMF.
A Bisocard CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Bisocard 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 Bisocard suppliers with CEP (COS) on PharmaCompass.
We have 18 companies offering Bisocard
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