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2026 CRBE SUMMIT EAST

Innovations in Controlled Release, Bioavailability Enhancement & Nano Drug Delivery Systems

May 12-13, 2026 - Crowne Plaza Princeton, Princeton, NJ

ATTEND             SPONSOR

2026 CRBE SUMMIT EAST

Innovations in Controlled Release, Bioavailability Enhancement & Nano Drug Delivery Systems

May 12-13, 2026 - Crowne Plaza Princeton, Princeton, NJ

ATTEND             SPONSOR

2026 CRBE SUMMIT EAST

Innovations in Controlled Release, Bioavailability Enhancement & Nano Drug Delivery Systems

May 12-13, 2026 - Crowne Plaza Princeton, Princeton, NJ

ATTEND             SPONSOR

Pharma / biotech can save 3o% on your seat with super early-bird pricing ($1100) + 3-for-the-price-of-2 group packs available. Offer ends in:

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The next generation of drug product development

and manufacturing technology is here…

Now in it’s 13th year, the popular 026 CRBE Summit East – Innovations in Controlled Release, Bioavailability Enhancement & Nano Drug Delivery Systems returns this May.

Connect with 160+ senior drug development innovators and uncover industry’s latest formulation, product development and delivery technologies for improving performance and manufacuring capabilities.

2026’s Summit covers Controlled & Modified Drug Release, Drug Bioavailability Enhancement and Nano Drug Delivery technologies and capabilities. 

✅ 2 full tracks of technical talks, panels and thought-provoking discussion sessions
✅ Network with 100’s of senior development, formulation and manufacturing attendees and solution providers
✅ Multiple exhibits, banquet lunches and dinners, workshops, exhibits, champagne giveaways and networking receptions
✅ Access all sessions post-Summit on-demand so you can relive your best moments
✅ Be part of our community of drug product development experts which will open many doors in the future.

40+

Industry-led Speakers

160+

Senior Attendees

2

Tracked Streams

14+

Networking Hours

18

Solution Providers

2026 Speakers Include

Mansoor A. Khan, PhD

Mansoor A. Khan, PhD

Dean & Distinguished Professor of Pharmaceutical Sciences & Ex CDER FDA

Texas A&M University

James DiNunzio, PhD

James DiNunzio, PhD

Executive Director & Distinguished Scientist

Merck & Co.

Indrajit Ghosh, PhD

Indrajit Ghosh, PhD

Scientific Director, Biologics Product Development

Bristol Myers Squibb

Liangfang Zhang, PhD

Liangfang Zhang, PhD

Professor, Department of Chemical and Nano Engineering

University of California San Diego

Karunakar Sukuru, PhD

Karunakar Sukuru, PhD

Global Vice President, Pharma Product Development & Head of Scientific Advisory

Catalent Pharma Services

Shabbir Lobo, PhD

Shabbir Lobo, PhD

Staff Scientist, Global Innovations and Product Development

Bayer

Amit Kale, PhD

Amit Kale, PhD

Executive Director, CMC/Drug Product, Pharmaceutical Development

Relay Therapeutics

Michael Grass, PhD

Michael Grass, PhD

Senior Director, Product Innovation

Bend Bioscience

Lipa Shah, PhD

Lipa Shah, PhD

Director, Novel Delivery Technologies

Novartis

Dave Miller, PhD

Dave Miller, PhD

Chief Scientific Officer

AustinPx

Anjali Agrawal, PhD

Anjali Agrawal, PhD

Executive Director, CMC & Product Supply

Novo Nordisk

Deb Das, PhD

Deb Das, PhD

Senior Associate Director & Science Fellow, Innovation & Product Development Lead

Bayer

Kush Patel, PhD

Kush Patel, PhD

Research Fellow, Oral Product Development

Pfizer

 Nicole Jarvi, PhD

Nicole Jarvi, PhD

Senior Scientist - Biologics & Biopharmaceutics, Sterile Product Development

Merck & Co.

Freddy Arce, PhD

Freddy Arce, PhD

Senior Scientist, Oral Solid Dosage

Bristol Myers Squibb

Nick DiFranco, MEN

Nick DiFranco, MEN

Senior Marketing Manager, Pharmaceutical Division

Gattefossé USA

Andrew Leithead, PhD

Andrew Leithead, PhD

Associate Principal Scientist, Discovery Pharmaceutical Sciences

Merck

Dhaval Patel, PhD

Dhaval Patel, PhD

Executive Director & Head, Formulation Development

PTC Therapeutics, Inc.

David Schoneker, PhD

David Schoneker, PhD

President

Black Diamond Regulatory Consulting, LLC

Wesley Tatum, PhD

Wesley Tatum, PhD

Senior Principal Engineer

Serán BioScience

Vivek Gupta, PhD

Vivek Gupta, PhD

Associate Professor, Pharmaceutical Sciences

St. John’s University

Zoe Wen, PhD

Zoe Wen, PhD

Principal Scientist, Formulation Development

Sanofi

Ali Rajabi-Siahboomi, PhD

Ali Rajabi-Siahboomi, PhD

Advisory, Leadership & innovation

ALi Pharma Solutions, LLC

Sebastian Escotet, PhD

Sebastian Escotet, PhD

Principal Scientist, Oral Formulation Sciences

Merck & Co.

Controlled and Modified Release

  • Oral Drug Delivery Systems
  • Long Acting Injectable Drug Delivery Systems
  • Transdermal Drug Delivery Systems
  • Modified release coating systems
  • Biodegradable and Biocompatible Polymers
  • Nanotechnology in Controlled Release
  • Pulmonary Drug Delivery Systems
  • The Role of Controlled Release in Optimizing Therapeutic Outcomes
  • Patient Centric / Pediatric Dose Development
  • 3D Printing in Controlled and Modified Release
  • Regulatory considerations
  • Continuous manufacturing of Controlled and Modified Release products
  • Continuous modified release coating systems
  • Continuous long-acting microsphere manufacturing

Bioavailability Enhancement

  • Formulation strategies for improved absorption of poorly soluble and/or poorly permeable drugs
    Solubility and dissolution enhancement techniques:
    – Lipid-Based formulations
    – Micronization
    – Nanomedicine
    – Nanocarriers
    – Spray Dried Dispersions (SDD)
    – Hot Melt Extrusion (HME)
    – Kinetisol
  • Biopharmaceutics classification system (BCS) and its implications
  • In vitro-in vivo correlations (IVIVCs)
  • Continuous manufacturing technologies for Bioavailability Enhancement

Continuous Manufacturing

  • Continuous biopharmaceutical manufacturing
  • Continuous manufacturing of oral solids
  • Spray Drying and Continuous Manufacturing of Pharmaceutical Materials
  • Melt Extrusion and Continuous Manufacturing of Pharmaceutical Materials
  • Continuous reactors for pharmaceutical manufacturing
  • Recent regulatory status in continuous manufacturing
  • Continuous Manufacturing equipment change over time
  • Capacity planning for continuous pharmaceutical manufacturing facilities
  • Continuous modified release coating equipment
  • Continuous fluid-bed coating
  • Continuous tablet-coating
  • Continuous lyophilization

2026 Sponsors & Exhibitors

Gattefosse
Gattefosse
Gattefosse
Gattefosse
Fluid Air
Gattefosse
Gattefosse
Gattefosse

Download The Controlled Release Previous Attendee List

Partnering with the 2026 Summit will also help you:

  • Enhance commercial relationships with existing clients through platform interaction, meetings, and discussing the latest opportunities
  • Raise your brand awareness to a captive and engaging audience, which most-of-all encompasses decision-making criteria
  • Elevate your profile amongst industry peers and developing a contact base through 1-2-1 networking sessions
  • Generate direct new business opportunities from senior-level attendees with decision-making criteria currently sourcing drug product development solutions

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Registration Pricing:

Super Early-Bird

Register Before April 17, 2026

Pharma / Biotech

$1100

3-for-2 Group Pack

$2200

CDMO / Vendor Registration

$3500

On-Demand

$595

Early-Bird Rate

Register Before May 8, 2026

Regular Attendance

$1400

3-for-2 Group Pack

$2800

CDMO / Vendor Registration

$3500

On-Demand

$595

ONSITE PRICING

Register May 9, 2026 Onwards

Regular Attendance

$1600

3-for-2 Group Pack

$3200

CDMO / Vendor Registration

$3500

On-Demand

$795

Access the 2025 Summit On-Demand Content for Free

The 2025 Summit  highlighted innovative strategies, approaches and platforms designed to overcome drug product development and delivery . From cutting-edge techniques such as elec­trospinning, mesoporous silica technology, 3D printing, physiochemical optimization, amorphous nanoparticle engineering, to sophisticated pharmacokinetic modeling, the Summit detailed a wide range of approaches. The ultimate objective is to help you save valuable time and resources while expediting the development of yor drug products.

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Registration