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2025 Summit on Innovations in Controlled Release, Bioavailability...
2025 Summit on Innovations in Controlled Release, Bioavailability Enhanceme
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Wednesday
, May 7
Brunswick Ballroom
8:55am •
Welcome and Chairperson’s Introduction & Opening Remarks
9:00am •
From Intermittent to Flow: SMART Data Integrity Lessons and Commonsense Driving Pharma’s Manufacturing Evolution
9:40am •
Spray Drying Digital Twin for Rapid and Efficient Process Development, Scale-up, and Tech-Transfer
10:10am •
Long-Acting Intravitreal Dexamethasone Implant: Process, Drug Release Mechanism and Bio-Predictive In Vitro Drug Release Testing
11:10am •
Implications of Solution Phase Phenomena and Nanodroplet Formation upon Dissolution of Amorphous Dispersions in Simulated and Aspirated Intestinal Media
11:40am •
Potential of Multi-particulate Techniques in Solidifying Self-Emulsifying Drug Delivery System
12:10pm •
Rapid Transfer of Existing Immediate Release Drug Product Across Manufacturing Lines, A Blueprint for Distributive Manufacturing
1:40pm •
Multiparticulates for Modified Release Systems
2:10pm •
Bioavailability Insights Case Study: Non-Standard Approaches to Improve Bioavailability
2:10pm •
Osmotic-Controlled Release Oral Tablets: Technology and Functional Insights
2:10pm •
From Molecule to Market: Navigating Solubility Challenges in Drug Development
2:40pm •
Leveraging an Ecosystem of Technologies to Accelerate Drug Development
3:30pm •
Product Performance Optimization through Accurate Technology Selection and Lipid-Based Formation
4:00pm •
Consumer-Centric Nasal Bioavailability Enhancement Formulation Development
4:30pm •
Beyond the Capsule: Unlocking the Full Potential of Lipid Excipients in Oral Solid Dosage Forms
4:50pm •
Synchrotron Computed Tomography Combined with AI-Based Image Analysis for the Characterization of Spray Dried Amorphous Solid Dispersion Particles
4:50pm •
Navigating the Nitrosamine Maze: Pursuit of Inhibitor Allies
Brunswick Prefunction
8:00am •
Registration Opens & Continental Breakfast for Attendees
10:40am •
Morning Networking Break in Exhibit Hall
12:40pm •
Networking Lunch
3:00pm •
Afternoon Networking Break in Exhibit Hall
5:20pm •
Chair’s Closing Remarks, Drinks Reception in Exhibit Hall and End of Day One
Thursday
, May 8
Brunswick Ballroom
9:00am •
Chairperson’s Welcome & Opening Remarks
9:00am •
Modified Release Technologies: Enhancing Therapeutic Effectiveness, Patient Compliance, and Product Lifecycle Management
9:30am •
Formulation Technologies for Tackling Solubility and Bioavailability Challenges
9:45am •
Case study: Leveraging Hot Melt Extrusion to Improve Bioavailability, Reduce Pill Burden, and Increase Shelf Life
10:15am •
Unlock the Secrets to Strategic Drug Product Design: Formulation Strategies Across the DCS
11:15am •
Lipid-Based Formulations: Maximizing the Delivery of Poorly Soluble Drugs
11:45am •
Streamlining Osmotic Tablet Development
12:15pm •
Solid Dispersions to Address Crystallinity
1:45pm •
Calculating pH-Solubility Profile and pHmax for Monoprotic Salts of Poorly Water-Soluble Weak Bases
2:15pm •
The Rise of Continuous Manufacturing: Melt Granulation and Melt Extrusion in Pharma
3:00pm •
Overcoming Bioavailability Barrier to Deliver Protein Degraders
3:30pm •
Continuous Manufacturing of Solid Dose Products: The Next Chapter
Brunswick Prefunction
10:45am •
Morning Networking Break in Exhibit Hall
12:45pm •
Networking Lunch
2:45pm •
Morning Networking Break in Exhibit Hall
4:00pm •
Chair’s Closing Remarks and End of Day Two
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May 7
-
8, 2025
Wednesday
, May 7
Thursday
, May 8
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Hyatt Regency New Brunswick, New Brunswick, NJ
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Brunswick Ballroom
Brunswick Prefunction
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Bioavailability Stream
Continuous Manufacturing Stream
General Session
Keynote
Morning Networking Break
RUTGERS CM SITE TOUR
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Dates
Wednesday
, May 7
Thursday
, May 8
Session Type
Bioavailability Stream
Continuous Manufacturing Stream
General Session
Keynote
Morning Networking Break
RUTGERS CM SITE TOUR
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