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Privacy PolicyPinsent Masons provides legal services globally via a number of entities. Most of the firm’s main IT systems are located in the UK and controlled by Pinsent Masons LLP. We are a data controller of the personal informatio
Manufacturing Strategy Development - GBI BiomanufacturingRead about GBI s manufacturing strategy development for process development, scale-up, cGMP manufacturing, through to regulatory filings and related services.
Project Management - GBI BiomanufacturingExplore GBI s project management method for keeping CDMO biologics projects on track and on budget in a transparent, proactive manner prioritizing the client.
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.
cGMP Clinical Commercial Manufacturing Services - GBI BiomanufacturiLearn about GBI s cGMP manufacturing capabilities for drug substances and drug products including monoclonal antibodies, vaccines, and antibody drug conjugates.
Analytical Method Development, Assay Verification, and CharacterizatioGBI’s protein characterization provides bioanalytical method development and assay verification services that follow current USP/EP guidance for therapeutics.
Bioconjugation Services - 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 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.
DSP Purification Development Services - GBI BiomanufacturingLearn more about GBI s proven track record of developing robust, scalable, and cost-effective protein downstream processes across many different biologics.
Stability Testing Services - GBI BiomanufacturingLearn about GBI s ICH stability testing parameters to determine if a drug substance or drug product s quality is altered over time by environmental factors.
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