01 1Zhejiang Starry Pharmaceutical Co., Ltd
01 1ACETOIODIDE
01 1China
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33208
Submission : 2019-04-09
Status : Active
Type : II
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A Acetyl iodide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acetyl iodide, including repackagers and relabelers. The FDA regulates Acetyl iodide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acetyl iodide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Acetyl iodide supplier is an individual or a company that provides Acetyl iodide active pharmaceutical ingredient (API) or Acetyl iodide finished formulations upon request. The Acetyl iodide suppliers may include Acetyl iodide API manufacturers, exporters, distributors and traders.
click here to find a list of Acetyl iodide suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Acetyl iodide DMF (Drug Master File) is a document detailing the whole manufacturing process of Acetyl iodide active pharmaceutical ingredient (API) in detail. Different forms of Acetyl iodide DMFs exist exist since differing nations have different regulations, such as Acetyl iodide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Acetyl iodide DMF submitted to regulatory agencies in the US is known as a USDMF. Acetyl iodide USDMF includes data on Acetyl iodide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Acetyl iodide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Acetyl iodide suppliers with USDMF on PharmaCompass.
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