Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
01 1AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN
02 1ALIVUS LIFE SCIENCES LIMITED Mumbai IN
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 2APOTEX PHARMACHEM INDIA PVT. LTD Bangalore IN
05 1ARCH PHARMALABS LIMITED Mumbai IN
06 1HETERO DRUGS LIMITED Hyderabad IN
07 1IPCA LABORATORIES LIMITED Mumbai IN
08 2KRKA, d.d., Novo mesto Novo mesto SI
09 1LUPIN LIMITED Mumbai IN
10 1Laboratorios Servier S.L. Toledo ES
11 1MATRIX PHARMACORP PRIVATE LIMITED Sangareddy District IN
12 1NINGBO MENOVO PHARMACEUTICAL CO., LTD. Ningbo Hi-Tech District CN
13 1ORIL INDUSTRIE Bolbec FR
14 1PIRAMAL PHARMA LIMITED Hyderabad IN
15 1ROLABO OUTSOURCING, S.L. Zaragoza ES
16 1ZHEJIANG CHANGMING PHARMACEUTICAL CO., LTD. Taizhou CN
17 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
18 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Taizhou CN
Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
Certificate Number : R1-CEP 2013-245 - Rev 02
Status : Valid
Issue Date : 2022-10-27
Type : Chemical
Substance Number : 2019
86
PharmaCompass offers a list of Perindopril Erbumine 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 Perindopril Erbumine manufacturer or Perindopril Erbumine supplier for your needs.
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A AKOS015841351 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AKOS015841351, including repackagers and relabelers. The FDA regulates AKOS015841351 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AKOS015841351 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 AKOS015841351 supplier is an individual or a company that provides AKOS015841351 active pharmaceutical ingredient (API) or AKOS015841351 finished formulations upon request. The AKOS015841351 suppliers may include AKOS015841351 API manufacturers, exporters, distributors and traders.
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A AKOS015841351 CEP of the European Pharmacopoeia monograph is often referred to as a AKOS015841351 Certificate of Suitability (COS). The purpose of a AKOS015841351 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of AKOS015841351 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of AKOS015841351 to their clients by showing that a AKOS015841351 CEP has been issued for it. The manufacturer submits a AKOS015841351 CEP (COS) as part of the market authorization procedure, and it takes on the role of a AKOS015841351 CEP holder for the record. Additionally, the data presented in the AKOS015841351 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the AKOS015841351 DMF.
A AKOS015841351 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. AKOS015841351 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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We have 16 companies offering AKOS015841351
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