White Papers

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 11, 2017
Sponsored Content
For years, the development of drugs for respiratory diseases have been relying on the administration of a new drug, mostly by inhalation and assessment by physiologic tests and questionnaires. More and more these new drugs are administered in fixed combinations.
Nov 01, 2017
Sponsored Content
Alleviate the burden of errors, non-compliance, and time-consuming discrepancy resolution with ART™. The industry's first truly holistic solution for Accountability & Reconciliation Tracking, providing full visibility into all IMP events.
Oct 31, 2017
Sponsored Content
Clinical trial agreement development has a tremendous impact on study start-up – integrating site-level budgets, payment terms, and Clinical Trial Management Systems set-up. By understanding the most important considerations for contract development and budget planning, you can execute a fully-integrated process that results in high-efficiency enabled contracts and payments.
Oct 27, 2017
Sponsored Content
What do ATM machines and eCOA have in common? Senior Scientific Advisor, Dr. Jill Platko, addresses this when discussing how to design an eCOA solution for senior populations.
Oct 27, 2017
Sponsored Content
Watch this on-demand webinar to learn the benefits and challenges of each modality used in clinical trials today, items to consider, and tips for successful eCOA modality selection.
Oct 27, 2017
Sponsored Content
Sandra “SAM” Sather is joined by Giga Smith from Coastal Carolina Health Care (CCHC) to discuss benchmarks from our 2017 eConsent Site Survey.
Oct 27, 2017
Sponsored Content
In this eConsent video, industry expert, Sandra "SAM" Sather, explains how the localisation process is easier to implement in an electronic informed consent (eConsent), and what study teams should consider as they design their eConsent solution.
Oct 03, 2017
Sponsored Content
By Marken
Direct-to-patient (DTP) services for clinical trials are growing in popularity due to their many benefits for patients and the pharma industry. With its flexible global network, highly trained personnel, supporting technology and extensive regulatory expertise, Marken offers efficient, compliant, cost-effective and personalised clinical trial logistic services.
Oct 01, 2017
Sponsored Content
By Rho
A protocol is the most important document in a clinical study as it is the foundation for subsequent operational, regulatory, and marketing objectives for the development program. This guide includes information on designing the study, drafting the synopsis, and minimizing the potential for amendments.
native1_300x100
lorem ipsum