White Papers

Apr 01, 2017
Sponsored Content
FIH studies that need to include woman will find that successful enrollment is achievable with the correct strategies. This paper explores challenges in recruiting women and strategies for improving the recruitment rates.
Mar 20, 2017
Sponsored Content
As sponsors of clinical trials become more discerning about the strengths of individual contract research organizations (CROs), strategic alliances between CROs offer access to shared efficiencies in new geographic areas.
Mar 10, 2017
Sponsored Content
Increasingly sensitive and sophisticated pharmaceuticals and the proliferation of new regulations have made temperature control a hot topic. These issues raise concerns within pharmaceutical companies as well as with regulators. Download Almac’s ‘An eye on temperature’ article to learn more.
Mar 01, 2017
Sponsored Content
By Marken
Numerous changes in the pharmaceutical industry have affected the nature of clinical trials, which in turn have led to the evolution of systems used for the supply of clinical trial materials.
Mar 01, 2017
Sponsored Content
By Rho
This paper provides recommendations for effective use of Special Protocol Assessments (SPA) for Phase 3 including strategies for a successful SPA, tips for optimal use, and End of Phase 2 meetings as an alternative.
Feb 28, 2017
Sponsored Content
Clinical trial sponsors have an obligation to provide clinical trial results to trial participants. The Trial Results Summaries Portal offers a new approach to patient engagement and education that empowers patients and improves patient-centric communications.
Nov 24, 2016
Sponsored Content
Bracket created an eBook that discusses the challenges with Alzheimer’s Disease and how the emergence of new approaches and investments in technology and research are paving a path forward.
Nov 08, 2016
Sponsored Content
Learn how genomics and advanced technology, such as RNA-Sequencing, empower the success of immuno-oncology drug development and biomarker discovery in our complimentary white paper.
Nov 08, 2016
Sponsored Content
Informed consent is more than just a form – it's a process. Regulators and industry groups are pushing for the adoption of electronic informed consent (eConsent) for the multitude of benefits it offer patients as well as sponsors and site teams, but the technology is so new, it can be hard to know where to start. Download our latest eBook, "The Essential Guide to Electronic Informed Consent," to learn how eConsent enhances the consent process.
Oct 05, 2016
Sponsored Content
At CRF Health, one of the most common concerns voiced by our clients is the migration of existing paper instruments to an electronic platform. Where do we start? How do we ensure a smooth migration? What can we do to ensure regulatory requirements are satisfied? If you share in these concerns, please download our latest eBook, "Paper to eCOA: A Guide to Migration," to learn the necessary steps and key considerations for a successful migration. Download the guide now to ensure your next migration process is straightforward and hassle-free.
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