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Are you looking to improve drug performance, bioavailability and patient adherence? Would you like to reduce dosage, cost and time-to-market?
Get involved today at the 2020 Global Drug Bioavailability Enhancement Summit and dramatically increase the performance and activity of your current and future drug products. 2020’s not-to-be missed Summit will connect industry leaders from both small molecule and biologics areas to address challenges at the interface between drug discovery and preclinical/clinical development. 2020’s Summit will share cutting edge research on the development, characterization and manufacture of formulations that span multiple modalities. Hear from 30+ senior drug bioavailability pioneers and network with 120+ senior drug development innovators and walk away with over 2 years of new drug formulation and bioavailability enhancement approaches strategies in just 2 days!
Don’t miss your chance to take advantage of the early-bird discounted registration which expires soon, as well as group packs for your team.
[2020 Featured Speakers Include]
Rakesh Dixit, PhD
President & CEO
Bionavigen
Ildiko Terebesi, PhD
Head, Early Formulation Development
Bayer
Wei Zhu, PhD
Senior Scientist, Biopharmaceutics & Speciality Dosage Forms
Merck & Co.
Rick Panicucci, PhD
Senior Vice President, CMC
QED Therapeutics
Dedong Wu, PhD
Senior Scientist, Pharmaceutical Science
AstraZeneca
Doug Nesta, PhD
Senior Director, Biopharmaceutical Product Sciences
GlaxoSmithKline
Dina Zhang, PhD
Senior Research Fellow
Merck & Co.
John Morrison, PhD
Senior Research Investigator
Bristol Myers Squibb.
Bob Prud'Homme, PhD
Professor and Director Program in Engr. Biology
Princeton University
Saileta Prabhu, PhD
Senior Director / Head, PKPD
Genentech
Indrajit Ghosh, PhD
Senior Principal Scientist, Pharmaceutical Science and Technology
Celgene Corporation
Phillip Snyder, PhD
Associate Director, Preclinical and Pharmaceutical Sciences
Vertex Pharmaceuticals
Industry-led Speakers
Senior Participants
Networking Hours
Tech Exhibitors
Attendees have access to:
- 30+ industry-led speaker faculty over 2 full days sharing innovative drug development take-home strategies
- 14+ hours of networking sessions and breaks over two full days to learn from network with pharmaceutical and biotech senior formulation, development and delivery professionals
- 120+ Senior Participants spanning pharma, biotech and specialty delivery & technology companies
- Dynamic Exhibition Hall with multiple leading formulation development, delivery, instrumentation and modeling experts
- Multiple innovative go-to-market & take-home strategies and learn 2 years of drug bioavailability strategies and approaches!
- Network with drug development’s innovators and join our growing community of drug commercialization professionals
You will learn:
- Precision medicine & healthcare delivery
- Developing differentiation, innovation, and long term growth strategies with life-cycle technologies
- Maximizing exposure for new compounds in early formulation development
- Product diversification and enhancement through pre-formulation technologies
- Enhancing the bioavailability of poorly water-soluble drugs: Oral lipid-based formulations
- Expediting time-to-market and reducing time-to-launch with physicochemical optimization
- Solution behavior of amorphous solid dispersions
- Expedited formulation development guided by biopharmaceutical modeling
- Nanosuspension for improving the bioavailability
- Early formulation screening in drug discovery
- 3D printing for biopharmaceuticals
- Enhancing patient adherence via drug delivery
- Innovative strategies around drug / device combinations
Join multiple pharmaceutical, biotech and academic professionals specializing in:
- Drug Delivery
- Pharmaceutics
- PK-PD
- Physiochemistry
- Formulation / Pre-Formulation
- Medicinal / Analytical / Solid state Chemistry
- Preclinical / Analytical Development
- Product Enhancement / Development
- CMC
- Regulatory Affairs
- Drug Discovery
- Life-Cycle / Portfolio Management
- Partnering, Licensing & Alliance Management
- Intellectual Property
- Toxicology
- Process R&D
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INTERESTED IN BECOMING A SPONSOR?
Registration Pricing:
Early-Bird
Register Before Dec 31st 2019
Conference Only
$1,895
Conference + 1 Workshop
$2,095
STANDARD PRICING
Register Before Jan 24th, 2020
Conference Only
$2,095
Conference + 1 Workshop
$2,295
ONSITE PRICING
Register At Event
Conference Only
$2,295
Conference + 1 Workshop
$2,495
WANT MULTIPLE FREE BIOAVAILABILITY ENHANCEMENT STRATEGIES?
The New Yorker, A Wyndham Hotel
Blog Posts:
Commercial Advances in Drug Delivery Systems for Peptide-Based Therapeutics
Beyond 2020, the global Peptide Therapeutics market is expected to eclipse $42 billion. This dramatic market increase is driven by both growing incidences of cardiovascular and metabolic diseases, and technological enhancements in peptide synthesis that include...
Understanding the Importance of Excipient Selection for Controlled Release
Controlled delivery formulations remain one of the favored tools for advancing the lifecycle of pharmaceutical products. A traditional strategy is to initially launch multiple daily doses of an immediate-release (IR) product, then reformulate into a once-daily...
Why Should you Consider Developing Controlled and Modified-Release Drug Products?
There are a number of pharmacological and economical benefits to developing controlled and modified release drug products. Following the 505(b)(2) pathway allows companies to make modest changes to an already approved drug and get continued market exclusivity for a...
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