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3rd Annual Global Drug Bioavailability Enhancement Summit
Wednesday, June 26, 2019
Thursday, June 27, 2019
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Most drugs on today’s market display poor solubility, but the use of modern solubilization technologies can improve a drug product's bioavailability and performance. Even the most promising API, monoclonal antibody or therapeutic peptide can only be turned into an effective and marketable drug if formulated in such a way that it is bioavailable.
Most of the drugs and APIs currently on the market are poorly water-soluble and need to have their bioavailability improved through the development of enabled formulations and patient-centric delivery mechanisms. Finding the solution that gives a particular drug the desired profile is still a major headache for pharmaceutical firms.
Additionally, biopharmaceutical firms hoping to develop oral delivery alternatives for injectable biologics will also need to work out how to ensure that their products are bioavailable, safe and effective. Small-and large-molecule therapeutics urgently need to overcome drug formulation and delivery challenges in order to improve bioavailability and therapeutic performance.
Curtis & Coulter’s 3rd Annual Global Drug Bioavailability Enhancement Summit will examine and showcase the industry’s latest formulation and delivery technologies for enhancing solubility and maximizing bioavailability. Learn directly from leading global formulation experts in both industry and academia on how to effectively develop poorly soluble drugs into scientifically unique, compliant, patient-centric formulations. Additionally, learn innovative strategies to significantly reduce product development timelines, brush up on the latest regulatory requirements and learn multiple innovative strategies to optimize and enhance your product portfolio.
Please note the 3rd Global Drug Bioavailability Enhancement Summit is co-located with the 3rd Oral Drug Formulation Innovations Summit. Attendees have access to BOTH events as a value add.
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