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Testimonials
  • "An excellent opportunity to hear the latest industry issues and talk to experts in the field. "
    Principle Scientist, Process Development, GSK
  • "Clever way to link case studies to our daily life as formulators: ideal mix between academic and applied "ready to use" practises."
    Formulation Research Director, Virbac

  • "Excellent venue, allowing several opportunities for cross fertilisation of ideas"
    Head, Analytical and Formulation Research, GSK

  • "well organised conference on drug delivery, with good mix of science and business tools"
    Director, formulation and process development, Merck Serono

  • "A complete update on formulation development"
    Head, Pharmaceutical Development, sigma tau

  • "a fantastic mix of top quality science and commercial presentations and top notch networking"
    Director of Operations, Critical Pharmaceuticals

The leading drug formulation and delivery professionals across Europe will be gathering to examine the latest technological developments and strategic advancements affecting the industry.

This year’s multi-streamed sessions include:

Small Molecule Formulation & Delivery

  • Successful Formulation Strategies in Achieving Novel Product Development
  • Improving bioavailability of poorly soluble compounds
  • Controlled release technologies

Biologics Formulation & Delivery

  • Preventing aggregation and ensuring stability in biologic formulation
  • Characterization of Biological Drug Products
  • Biologic combination products – technical development and commercial drivers

Medical Device Development

  • Implants and biodegradable device platforms in enhancing drug delivery
  • Balancing device technology enhancement with patient usability
  • Patient & technical considerations for device design

Emerging Technologies

  • Applications of nanotechnology and particle size reduction in combating issues of bioavailability
  • Maximising drug release control with polymer technologies
  • Exploring different routes of administration in enhancing macromolecule delivery

Out-sourcing and in-licensing

  • Successfully sourcing new technologies from both academia and the industry
  • Successful partnership strategies in approaching, managing and maintaining effective partnerships

Regulations and Compliance

  • Regulatory viewpoint on QbD in pharmaceutical development
  • Effectively responding to the Paediatric Implementation Plan (PIP)

Click here to view World Drug Delivery and Formulation 2012 programme