Two day Program: 5th Annual Controlled and Modified Drug Release Summit (Philadelphia, PA, United States - September 5th-6th, 2018) - ResearchAndMarkets.com

DUBLIN--()--The "5th Annual Controlled and Modified Drug Release Summit" conference has been added to ResearchAndMarkets.com's offering.

This intensive 2-Day program will share innovative controlled and modified drug release strategies that will benefit your current and future product pipelines.

Learn directly from industry's leading experts and hear unique case study sessions and take-home examples to enhance your product pipeline. Gather insights into the latest technologies and methods in improving drug release mechanisms, maximizing exposure, and reducing time-to-market. Additionally, this must-attend event will showcase the latest regulatory guidance updates and the implications for the industry.

Topics Include:

  • Localized & targeted delivery
  • Pediatric dosage forms & delivery
  • QBD Strategy
  • Novel alliance management strategies
  • Enhancing patient adherence for drug delivery
  • Evaluating innovations in oral drug formulation and delivery technologies
  • Implementing innovative strategies around drug / device combinations
  • Advances in ocular delivery
  • Parenteral routes of administration
  • Topical and Transdermal Delivery
  • Combining In-Vivo animal models with physiologically-based PBPK modeling
  • Modified release technologies for product lifecycle extensions

Benefits of Attending:

  • 70+ Industry-led Speakers
  • 200 Senior Participants
  • 10+ Networking Hours

Engage in dynamic conversation with your industry peers at our multiple networking sessions, and takeaway novel controlled and modified release strategies, which could speed up time to market and save your organization millions.

Who Should Attend:

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

For more information about this conference visit https://www.researchandmarkets.com/research/vzvfv2/two_day_program?w=4

Contacts

ResearchAndMarkets.com
Laura Wood, Senior Manager
press@researchandmarkets.com
For E.S.T. Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900
Related Topics: Drug Delivery

Contacts

ResearchAndMarkets.com
Laura Wood, Senior Manager
press@researchandmarkets.com
For E.S.T. Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900
Related Topics: Drug Delivery