Veranova: A CDMO that manages complexity with confidence.
01 1Veranova
02 1Abbott Laboratories
03 1Boehringer Ingelheim GmbH
04 2Cambrex Corporation
05 1Chattem Chemicals, Inc
06 1Cody Laboratories, Inc.
07 1Curia
08 1Fujifilm Diosynth Biotechnologies
09 2Mallinckrodt Pharmaceuticals
10 1Merck & Co
11 1Yichang Humanwell Pharmaceutical
12 1Blank
Veranova: A CDMO that manages complexity with confidence.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5038
Submission : 1983-08-15
Status :
Type : II
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A INNOVAR-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of INNOVAR-1, including repackagers and relabelers. The FDA regulates INNOVAR-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. INNOVAR-1 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 INNOVAR-1 supplier is an individual or a company that provides INNOVAR-1 active pharmaceutical ingredient (API) or INNOVAR-1 finished formulations upon request. The INNOVAR-1 suppliers may include INNOVAR-1 API manufacturers, exporters, distributors and traders.
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A INNOVAR-1 DMF (Drug Master File) is a document detailing the whole manufacturing process of INNOVAR-1 active pharmaceutical ingredient (API) in detail. Different forms of INNOVAR-1 DMFs exist exist since differing nations have different regulations, such as INNOVAR-1 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A INNOVAR-1 DMF submitted to regulatory agencies in the US is known as a USDMF. INNOVAR-1 USDMF includes data on INNOVAR-1's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The INNOVAR-1 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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