2nd Controlled & Modified Drug Release 2015

2nd Controlled & Modified Drug Release 2015 is a conference dedicated to Novel Formulation Approaches, Delivery Technologies, Regulatory Updates & Strategies to Accelerate Drug Product Time-To-Market.

• New approaches in modified release / modeling & simulation in modified release
• FDA guidance on pharmacokinetics and clinical evaluation of sustained & modified release dosage forms
• Pre-investment in control release
• Right conditions for IVIVC correlation
• Dissolution applications within controlled release
• In-licensing / out-licensing strategy
• Application of in-vivo and in-silico modeling
• Quality by Design Example for. Generic Modified Release Drug Products
• Techniques for drug delivery: Systems and targeted drug delivery
• Next generation products
• Topical and Transdermal Delivery
• Parenteral controlled & sustained release
• New formulations hot-melt extrusion technology development to optimize sustained delivery
• Rational design of drug delivery systems for poorly water soluble drugs

Who should Attend

Attendees with responsibilities in:

• Pharmaceutics
• Drug Delivery
• Physiochemistry
• PK-PD
• Pre-Formulation
• Formulation
• Analytical
• Medicinal
• Preclinical
• Solid state Chemistry
• Product Enhancement
• Analytical Development
• CMC
• Development
• Drug Discovery
• Regulatory Affairs
• Partnering
• Life-Cycle / Portfolio Management
• Intellectual Property
• Licensing & Alliance Management
• Process R&D
• Toxicology