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API SUPPLIERS
Shandong Loncom is an R&D-focused manufacturer of Anti-cancer APIs.
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Listed Suppliers
Shandong Loncom is an R&D-focused manufacturer of Anti-cancer APIs.
About the Company : Established in May 2012, Shandong Loncom Pharmaceutical is a wholly owned subsidiary of Shandong Bestcomm Pharmaceutical Co., Ltd. Located in the Qihe Economic Development Zone, Sh...
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PharmaCompass offers a list of YDSAJOSZKLMHFJ-ZCFIWIBFSA-N 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 YDSAJOSZKLMHFJ-ZCFIWIBFSA-N manufacturer or YDSAJOSZKLMHFJ-ZCFIWIBFSA-N supplier for your needs.
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A Levornidazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levornidazole, including repackagers and relabelers. The FDA regulates Levornidazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levornidazole 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 Levornidazole manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levornidazole supplier is an individual or a company that provides Levornidazole active pharmaceutical ingredient (API) or Levornidazole finished formulations upon request. The Levornidazole suppliers may include Levornidazole API manufacturers, exporters, distributors and traders.
click here to find a list of Levornidazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Levornidazole 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 Levornidazole 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 Levornidazole GMP manufacturer or Levornidazole GMP API supplier for your needs.
A Levornidazole CoA (Certificate of Analysis) is a formal document that attests to Levornidazole's compliance with Levornidazole specifications and serves as a tool for batch-level quality control.
Levornidazole CoA mostly includes findings from lab analyses of a specific batch. For each Levornidazole 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.
Levornidazole may be tested according to a variety of international standards, such as European Pharmacopoeia (Levornidazole EP), Levornidazole JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Levornidazole USP).
