White Papers

Jan 04, 2018
Sponsored Content
By WIRB
- Discussion of common challenges in clinical trials management - How to expedite the delivery of clinical trial contract negotiation. - Why methodical, accurate CTA preparation and budget development is key.
Jan 01, 2018
Sponsored Content
Informed consent is more than a form, it's a process. Regulators are pushing for the adoption of electronic informed consent (eConsent) for the benefits it offers patients, sponsors, and site teams. Download this guide to learn more about the newest technology in clinical trials.
Dec 18, 2017
Sponsored Content
What are connected devices and how can they be best used to advance the treatment of chronic conditions? Watch this webinar to learn how to transform your clinical trials with the latest tech solutions.
Dec 18, 2017
Sponsored Content
One of the largest sources of delay in clinical trials is difficulty to recruit. Once you obtain a subject, it's important that they remain engaged for the duration of the trial. Watch this video to learn how sites can better retain their subjects and keep them more compliant with electronic Clinical Outcome Assessments (eCOA).
Dec 01, 2017
Sponsored Content
This eBook is an introduction for researchers considering making the switch from traditional paper-based processes to an electronic Clinical Outcome Assessment (eCOA) solution when collecting data in vaccine clinical trials.
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
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.
Sep 21, 2016
Sponsored Content
One of the most common concerns voiced by clinical trial sponsors and CROs 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.
Aug 31, 2016
Sponsored Content
In this eBook, industry leaders Validic, Quintiles and Duke Clinical Research Institute explore the four categories of digital health technologies--wearable fitness devices, clinical devices, sensors and applications—and discuss what each category includes, endpoints they collect and how they’re being used in trials today.
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