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Found 47324 results for any of the keywords fill finish. Time 0.009 seconds.
Aseptic Fill Finish - GBI BiomanufacturingExplore GBI s sterile fill finish capabilities and process, including our ISO5 filling suite and details about our regulatory compliance and specialized fills.
World Pharma Today - Magazine for the C-level Pharma ExecutivesWorld Pharma Today is a leading Magazine featuring latest industry developments for the Pharmaceutical C-level executives.
Drug Product Manufacturing - AlcamiAlcami offers comprehensive drug product manufacturing and support services with DEA-certified facilities and FDA/EMA-approved operations.
DSP Purification Development - GBI BiomanufacturingLearn more about GBI s proven track record of developing robust, scalable, and cost-effective protein downstream processes across many different biologics.
cGMP Cell Banking Services - GBI BiomanufacturingRead about GBI s full array of cGMP-compliant cell banking services for short- or long-term storage for research or manufacturing including RCB, MCB, and WCB.
Bioconjugation - GBI BiomanufacturingGBI has performed over 50 bioconjugation projects involving process development and validation scale-up cGMP manufacturing of multi-gram antibody drugs and others.
cGMP Clinical Commercial Manufacturing - GBI BiomanufacturingLearn about GBI s cGMP manufacturing capabilities for drug substances and drug products including monoclonal antibodies, vaccines, and antibody drug conjugates.
Biopharmaceutical CDMO - GBI - Formerly Goodwin Biotechnology Inc.Learn about GBI, a biopharmaceutical CDMO based in Florida that aims to eliminate manufacturing risk for companies developing complex biologic therapeutics.
Upstream Processing Cell Culture Development - GBI BiomanufacturingExplore GBI s offering of robust and reproducible cell culture upstream process development services for producing complex therapeutic protein drug candidates.
Regulatory CMC Support - GBI BiomanufacturingConcerned about regulatory and CMC support for your drug candidate? Learn more about GBI s long experience with IND filings and FDA type II Drug Master Files.
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