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2025 Summit on Innovations in Controlled Release, Bioavailability Enhancement & Continuous Manufacturing

May 7-8, 2025 - Hyatt Regency New Brunswick, New Brunswick, NJ

REGISTER NOW             2025 AGENDA

2025 Summit on Innovations in Controlled Release, Bioavailability Enhancement & Continuous Manufacturing

May 7-8, 2025 - Hyatt Regency New Brunswick, New Brunswick, NJ

REGISTER NOW             2025 AGENDA

2025 Summit on Innovations in Controlled Release, Bioavailability Enhancement & Continuous Manufacturing

May 7-8, 2025 - Hyatt Regency New Brunswick, New Brunswick, NJ

REGISTER NOW             2025 AGENDA

Planing to attend? Save $200 on your ticket with super early-bird pricing ($1200) + 3-for-the-price-of-2 group packs available. Offer ends in:

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Registered To Attend the 2025 Summit this week?

The next generation of drug product development

and manufacturing technology is here…

Now in it’s 11th year, the popular 2025 Summit on Innovations in Controlled Release, Bioavailability Enhancement & Continuous Manufacturing 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.

2025’s Summit covers Controlled & Modified Drug Release, Drug Bioavailability Enhancement and Continuous Manufacturing 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

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

2025 Sponsors & Exhibitors

Fluid Air
Gattefosse
Gattefosse
Gattefosse
Gattefosse
Gattefosse
Fluid Air
Gattefosse
Gattefosse
Gattefosse
Gattefosse
Gattefosse

Download The Controlled Release Previous Attendee List

Partnering with the 2025 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 May 2, 2025

Regular Attendance

$1200

3-for-2 Group Pack

$2400

On-Demand

$595

Early-Bird Rate

Register Before May 6, 2025

Regular Attendance

$1400

3-for-2 Group Pack

$2800

On-Demand

$595

ONSITE PRICING

Register May 7, 2025 Onwards

Regular Attendance

$1600

3-for-2 Group Pack

$3200

On-Demand

$795

Access the 2024 Summit On-Demand Content for Free

The 2024 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