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2025 Controlled & Modified Drug Release Summit

May 14-15, 2025

Hyatt Regency Princeton, Princeton, NJ

Planning to attend? Save 45% on your ticket with super early-bird pricing ($1095). 3-for-2 packs available also. Offer ends in:

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The next generation of drug and therapeutic delivery is here…

Attend and connect with 160+ senior drug development innovators this May and uncover industry’s latest formulation and delivery technologies for improving drug product performance and developing next-gen products.

Uncover a multitude of new product development strategies, formulation approaches, delivery technologies in just 2 days. Likewise, access all session content for your team post-Summit via our on-demand portal. Benefit from 40+ expert sessions and panels.

That’s not all; attendees get access to the 2024 Global Drug Bioavailability Enhancement Summit and Continuous Manufacturing Summit – all under one roof!

Register early & save 60% on your seat. Attending 2025’s Summit might just be the best decision you make this year!

40+

Industry-led Speakers

160

Senior Participants

12+

Networking Hours

16

Tech Exhibitors

2024 Speakers Included

Joe Della Rocca, PhD

Joe Della Rocca, PhD

Associate Principal Scientist

Merck

Anand Uhbe, PhD

Anand Uhbe, PhD

Senior Scientist (II), Sterile Liquids Product Development

Abbvie

Dipy Vasa, PhD

Dipy Vasa, PhD

Principal Scientist, Drug Product Dev

Pfizer

Ryan Pelis, PhD

Ryan Pelis, PhD

Sr. Principal Scientist, Pharmacokinetic Sciences

Novartis

Kellyn Zagaja, PhD

Kellyn Zagaja, PhD

Principal Scientist, Drug Product Design

Pfizer

Siddharth S. Kesharwani, PhD

Siddharth S. Kesharwani, PhD

Biopharmaceutics Scientist

Sanofi

Indrajit Ghosh, PhD

Indrajit Ghosh, PhD

Scientific Director, Biologics Product Development

Bristol Myers Squibb

Aruna Railkar, PhD

Aruna Railkar, PhD

Senior Research Fellow

Quotient Sciences

Seth Forster, PhD

Seth Forster, PhD

Associate Principal Scientist

Merck

Girish Nihalani, PhD

Girish Nihalani, PhD

Research Fellow, Product Development

Teva Pharmaceuticals

Liliana Miinea, PhD

Liliana Miinea, PhD

Global Technology Manager, Pharmaceutical Excipients

Lubrizol

Kelly Zhang, PhD

Kelly Zhang, PhD

Senior Scientist, Analytical Enabling Capabilities – MBC | Analytical Research & Development

Merck

Misha Murashov, PhD

Misha Murashov, PhD

Assoc Prin. Scientist, Sterile & Specialty Products BDB

Merck

Prajwal Thool

Prajwal Thool

Scientist III, Drug Product Development

Genentech

Zafar Iqbal, PhD

Zafar Iqbal, PhD

Vice President & Head of Pharmaceutical Development

Glatt Group

Jim Baxter

Jim Baxter

NA Technical Business Development Manager

Lubrizol Life Science

Firouz Asgarzadeh, PhD

Firouz Asgarzadeh, PhD

President of Consulting Services

OSD Pharmaceutical Solutions

Vivek Gupta, PhD

Vivek Gupta, PhD

Associate Professor, Pharmaceutical Sciences

St. John’s University

Erica Schlesinger, PhD

Erica Schlesinger, PhD

Vice President of Technical Development

Seran Biosciences

Ketan Patel, PhD

Ketan Patel, PhD

Associate Professor of Pharmaceutics

St. John’s University

  • High Dose Subcutaneous Delivery: Roadmap from Pre-clinical to Launch
  • How To Accelerate Drug Product Optimization: Integrated Program Delivery using Translational Pharmaceutics
  • Percolation Behavior in an Immediate Release Tablet Dosage Form
  • Long-Acting Implant Product Development
  • The competences and Intricacies of Fluid Bed Technologies
  • Formulation of LAI: Understanding what Attributes Control Injectability
  • The Impact of Excipient Selection on Modified Release Profiles
  • Co-Excipient Strategies for Controlled Release Formulations
  • Oral Delivery of Peptides: Challenges and Opportunities
  • Advancing Oral Modified Delivery for Rare Diseases via Lipid Based formulations
  • Streamlining SC Biologics Drug Development
  • Using PBPK Modeling for Risk Assessment in Drug Product Development
  • Efficient New Tools for Solubility Enhancement and Lifecycle Management
  • High Dose Subcutaneous Delivery: Roadmap from Pre-clinical to Launch
  • Translational Formulation Approaches for the Oral Delivery of eRo5/bRo5 – Molecules
  • Strategies for ASD Formulation Development
  • Leveraging Melt-Spray-Congeal Microspheres as a Versatile, Patient-centric Oral Multiparticulate Platform
  • Cellular Model of the Oral Lymphatic Absorption Pathway
  • Topical Ophthalmic Drug Delivery: Insights from Marketed Products
  • And much more..

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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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Attendee Pricing

Super Early-Bird

Register before
Oct 18, 2024
In-Person Summit

$1095

Virtual Summit

$449

Early-Bird

Register before
April 25, 2025
In-Person Summit

$1,795

Virtual Summit

$549

Standard Pricing

RegisterApril 26, 2025 Onwards 

In-Person Summit

$1,995

Virtual Summit

$599

Access 2024 Summit On-Demand Summit Content here

2024 Bioavailability and Controlled Release Talks On-Demand Access

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