White Papers

Sep 01, 2017
Sponsored Content
By Almac
TempEZ™ offers full visibility of your temperature data from any stakeholder within your clinical or commercial supply chain including numerous temperature monitor brands. Almac are first to market a single platform that links data from a monitor, shipment, drug product and stability data while providing a quality approved process for controlled adjudication and excursion decisions.
Aug 28, 2017
Sponsored Content
New technologies are changing oncology research – not only for cancer researchers but for patients. This paper explores the potential of liquid biopsies across diagnostics, therapy monitoring and disease recurrence from a clinical development point of view.
Aug 18, 2017
Sponsored Content
Electronic Clinical Outcome Assessment (eCOA) solutions change the way cancer patients contribute to finding a cure. Discover how eCOA allows seriously ill cancer patients to participate in clinical trials by offering them the ability to submit their data remotely, from the comfort of home, or at the hospital while receiving care.
Aug 18, 2017
Sponsored Content
Clinical data management (CDM) is the process of collecting, cleaning, and managing subject data in compliance with regulatory standards. Data managers: learn about the latest technology in clinical research, including eCOA, and how it can be used to collect the most robust, clean, complete and defensible data to support clinical trials.
Aug 18, 2017
Sponsored Content
Electronic Informed Consent (eConsent) is the next big technological innovation in clinical trials. 146 respondents from 100 biotech, pharmaceutical, CRO, and IRB organizations shared their experiences, expectations, and ideas about the future of eConsent. Whether you’re just starting to consider eConsent or ready to expand adoption, download this report for industry insights.
Aug 18, 2017
Sponsored Content
As a follow-up to our 2017 State of eConsent industry report, CRF Health gathered site staff opinions regarding the impact that the paper-based informed consent process has on participant understanding, recruitment and retention. Feedback was collected from 105 respondents in roles including study coordinator, CRA, investigator, and researcher.
Aug 18, 2017
Sponsored Content
Bring Your Own Device (BYOD) is a growing topic in clinical trials. But what factors should be considered before implementing this approach on your next study? Download this eBook to learn more about the 9 key factors every study team should evaluate.
Aug 07, 2017
Sponsored Content
Pharmaceutical manufacturers have long struggled to create an efficient clinical trial process for faster approval. The root cause of most failures is a lack of efficacy data to support clinical trial claims. Subpar data can be directly tied back to an inability to track and report patient adherence to drug protocol.
Aug 01, 2017
Sponsored Content
By Rho
The failure rate of clinical studies in depression is high, and placebo response is often blamed. This article discusses why there is more to the story than placebo response.
Jul 27, 2017
Sponsored Content
Download the Veeva 2017 Unified Clinical Operations Survey Report to find out the needs, barriers, and opportunities for unifying the clinical trial process including EDC, CTMS, eTMF, and study start-up.
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