The 2nd annual World Orphan Drug Congress showcases drug development, new drug discovery and innovations related to rare diseases.
*** Places are selling out fast! *** Over 200 delegates already confirmed ***
Companies already attending include:
Register now to meet these companies »
The World Orphan Drug Congress is the industry-led Orphan Drug conference tackling global trends, market access and collaborations from big pharma, orphan specialists and patient organisations to impact rare diseases.
| Register to attend The World Orphan Drug Congress » |
See full conference programme » |
Download the brochure » |
Come to The World Orphan Drug Congress 2011 and discover:
- The international collaborative initiatives spurring the next generation of rare disease treatments
- Best practice for achieving reimbursement and market access for your orphan drug
- How to maximise the commercial potential of an orphan drug through expansion into multiple indications
- The importance of patient partnerships to ensuring successful orphan drug development
- New and cutting edge platforms for creating global rare disease patient registries
- How to successfully translate research into approved rare disease treatments
- Innovative case studies of clinical trials designed to overcome regulatory challenges of orphan drug approval
You’ll come away with great new ideas to do better business.
Register for The World Orphan Drug Congress »
Download Sponsorship Prospectus »
|
Hear from an elite speaker faculty including leading executives from:
- Pfizer
- GSK
- Genzyme
- Prosensa
- Amicus Therapeutics
- Protalix
- Shire HGT
- Amsterdam Molecular Therapeutics
- Celgene
- Alexion Pharmaceuticals
- PTC Therapeutics
- Santhera Pharmaceuticals
- Swedish Orphan Biovitrum
- Genetic Alliance
- Genethon
- Rare Disease UK
- AKU Society
- euro-Ataxia
- Behcet’s Syndrome Society
- CheckOrphan
- NIH
- European Commission
See full speaker list »
Register for The World Orphan Drug Congress »
|
The World Orphan Drug Congress 2011 focuses on:
- Openly debating the value related pricing of orphan drugs
- Determining a centralised mechanism to facilitate uniform patient access to orphan drugs
- Best practice to establish successful collaborations between patient groups and industry
- The need for comprehensive patient registries for all rare diseases
- Innovative clinical trials and market approval strategy
- Crucial lessons learnt from organisations long established and those that are entering the orphan drug market
If you need to know the latest innovations in these areas you must attend.
Register now »
Download Sponsorship Prospectus »
|
 |
 |
 |
Who should attend:
- Regulatory Affairs / Strategy
- Public Policy / Governmental Affairs
- Clinical Research / Development
- Scientific / Medical Affairs
- Corporate / Business Development
- CxO (Executive, Scientific, Operating)
Register for The World Orphan Drug Congress »
Download the brochure »
|
Who should sponcor:
- Regulatory Affairs / Strategy
- Public Policy / Governmental Affairs
- Clinical Research / Development
- Scientific / Medical Affairs
- Corporate / Business Development
- CxO (Executive, Scientific, Operating)
Download the brochure »
Register for The World Orphan Drug Congress »
|
 |