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Most Recent Flipbooks
Integrating Expertise For Product Success
Creating aligned and integrated physician and payer-focused value propositions
What Makes a Good Evidence Generation Plan?
This article will introduce some of the key factors and considerations for a successful evidence generation plan with further articles presenting additional details on specific components of the EGP.
Early Economic Modelling To Inform Decision Making
Innovative trial design Health Economics Webinar PPT
Closing the minority gap maximizing ethnic diversity in clinical trials article_FINAL
This topical article examines the role of the CRO in using culturally specific strategies to engage under-represented patient populations, in order to boost trial recruitment.
HTAi Poster_The Furture Model of Oncology Reimbursement
HTAi Poster_Future Trends for Managed Access in UK
The Resurrection of the Cost-Minimization Approach in England
Your Money or Your Life? Are Price Negotiations HTA Best Practice?
The Impact of pCODR Coming Under the Remit of CADTH - 3 Year Update
Orphan Diseases Translating Expedited Regulatory approval into Reimbursement success article
Innovative Clinical Trial Designs — Welcomed By Regulators But What About The Payers?
Presentation Slides: Early Engagement Strategies Webinar
Promoting the patient voice in evidence generation and global market-access planning
Presentation from the Medical Affairs Leaders Forum, London. February 27 - March 01, 2018
Safety Services: A tailored solution to support the needs of large companies
What to look for in a partner to support biosimilar initiatives
This article looks at some of the trends in biosimilars, including three key errors you need to avoid. Particularly, as it pertains to underestimating your risk management plan.
The Importance of QPPVs in Pharmacovigilance
Ian Kovacs, Head of QPPV & Safety Consulting at PAREXEL answers five key questions about the key role of a QPPV and why you should consider outsourcing.
A real life pharmacovigilance case story
How to implement a flexible and scalable pharmacovigilance model to transition a product from one company to another.