01 1AREVIPHARMA GMBH Radebeul DE
02 1EVONIK DEGUSSA GMBH Essen DE
03 1HAS HEALTHCARE ADVANCED SYNTHESIS SA Biasca CH
04 1MAITHRI LABORATORIES PRIVATE LIMITED Gaddapotharam Village IN
05 1PATHEON AUSTRIA GMBH & CO. KG Linz AT
06 1Procos S.P.A. Cameri IT
01 6Pyridostigmine bromide
01 1Austria
02 2Germany
03 1India
04 1Italy
05 1Switzerland
01 1Expired
02 5Valid
Certificate Number : CEP 2008-111 - Rev 03
Status : Valid
Issue Date : 2024-05-06
Type : Chemical
Substance Number : 1255
Certificate Number : R1-CEP 2001-348 - Rev 04
Status : Valid
Issue Date : 2022-03-01
Type : Chemical
Substance Number : 1255
Certificate Number : CEP 2021-085 - Rev 01
Status : Valid
Issue Date : 2024-05-03
Type : Chemical
Substance Number : 1255
Certificate Number : R1-CEP 2003-117 - Rev 03
Status : Valid
Issue Date : 2016-12-15
Type : Chemical
Substance Number : 1255
Certificate Number : CEP 2009-211 - Rev 01
Status : Valid
Issue Date : 2023-11-17
Type : Chemical
Substance Number : 1255
Certificate Number : R0-CEP 2005-139 - Rev 03
Status : Expired
Issue Date : 2007-12-05
Type : Chemical
Substance Number : 1255
89
PharmaCompass offers a list of Pyridostigmine 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 Pyridostigmine manufacturer or Pyridostigmine supplier for your needs.
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A DSSTox_RID_77069 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_RID_77069, including repackagers and relabelers. The FDA regulates DSSTox_RID_77069 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_RID_77069 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A DSSTox_RID_77069 supplier is an individual or a company that provides DSSTox_RID_77069 active pharmaceutical ingredient (API) or DSSTox_RID_77069 finished formulations upon request. The DSSTox_RID_77069 suppliers may include DSSTox_RID_77069 API manufacturers, exporters, distributors and traders.
click here to find a list of DSSTox_RID_77069 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DSSTox_RID_77069 CEP of the European Pharmacopoeia monograph is often referred to as a DSSTox_RID_77069 Certificate of Suitability (COS). The purpose of a DSSTox_RID_77069 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DSSTox_RID_77069 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DSSTox_RID_77069 to their clients by showing that a DSSTox_RID_77069 CEP has been issued for it. The manufacturer submits a DSSTox_RID_77069 CEP (COS) as part of the market authorization procedure, and it takes on the role of a DSSTox_RID_77069 CEP holder for the record. Additionally, the data presented in the DSSTox_RID_77069 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DSSTox_RID_77069 DMF.
A DSSTox_RID_77069 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DSSTox_RID_77069 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 DSSTox_RID_77069 suppliers with CEP (COS) on PharmaCompass.
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