Keynote Speaker

Gain Unique Insight from Top Industry Experts:

Advance your Drug Delivery Systems and Improve Patient Compliance to Increase your Market Share

As the global drive to streamline public services and cut healthcare costs intensifies, healthcare professionals are under pressure to implement patient self-management strategies wherever possible.

Alternative drug delivery systems are a perfect solution to allow patients to administer drugs at home, which has lead to a 10% year on year growth in the pre-filled syringes market

So, what’s your strategy for product differentiation?

The industry does still face several hurdles before developing the perfect pre-filled syringe solution, particularly with the advent of polymer based syringes. There is a now a fundamental question of glass vs. plastic and how to assess the subsequent product-container interactions.

Pharma IQ’s inaugural Innovation in Pre-Filled Syringes and Injectable Technologies conference, takes place in Munich from 8th- 9th March 2011. It is Europe’s only event that brings you interactivity and case studies exclusively from experts in the biotech and pharma industry, providing you with a unique opportunity to share best practice and openly network with your peers.

Download the brochure here for more details



EXCLUSIVE CASE STUDY

If you’re struggling to detect the leachable profile of your product we have an unmissable EXCLUSIVE CASE STUDY to share with you from Prof. Dr. Tudor Arvinte from the University of Geneva, who has designed, developed and patented a brand new, non-invasive method of detecting leachables in vials and syringes – hear first hand how this will significantly reduce your time and cost of development.


Key take home points:

  • Predict and minimise product container interactions during formulation development and understand the considerations for biological formulations
  • Improve the efficacy of your development and manufacturing processes by applying QbD and risk assessment principles
  • Take the next step to guaranteeing 100% syringe integrity through evaluating the most effective container closure testing systems
  • Enhance patient compliance by taking a user focused approach to device development and striking the balance between available and useful technologies when designing auto-injectables
  • Get a comprehensive insight into the different regulatory requirements for pre-filled syringe approval for both new and existing products – don’t miss the case studies form both perspectives!

What others have to say about Pharma IQ clinical trial events

Very good selection of speakers from all relevant areas of expertise.
Novartis Pharma
Great to have a day of practical projects & big pharma. Extremely valuable.
Genentech
Very eye-opening as to what others are doing in this area.
GlaxoSmithKline
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