Shifting from Paper to Digital Patient Consent
Charles Sydnor, CCRA, ACRP-CP, project manager at Crofoot, discusses how offering a digital patient experience in trials enables the site to provide better patient care.
Protecting Patients in COVID-19 Vaccine Clinical Trials
Michele Russell-Einhorn, Chief Compliance Officer at Advarra discusses safety, speed, and ethics in COVID-19 vaccine trials.
News Notes (January & February)
A compilation of recent notable news developments that pertain to the clinical trials industry.
News Notes (November)
News Notes (October)
New Centre for Medicines Research Report from Clarivate Indicates Drug Development Timelines are Shortest Since 2013
Pharmaceutical R&D industry report provides insights into what’s behind decline in global NME outputs and reveals implications of decreased projected expenditures.
News Notes
ACT Online
A compilation of ACT's most popular content from the previous month plus a look at upcoming webcasts.
W2O Releases Research on Consumer Attitudes Toward Privacy of Personal Health Data
W2O has announced findings from a research study on consumer attitudes toward data privacy, specifically personal health data.
Phesi Powers Data-Driven Clinical Trials Through Addition of New Country Selection Functionality to ClinSite
Phlexglobal Launches End-to-End TMF Solution
Raremark launches Xperiome Platform
LabCorp's Drug Development Business, Covance, Acquires GlobalCare
Me, We, And RWE: The Importance of Designing for the Patient First
In this Q&A, Helen Matthews, Jessica Morris, and Bruce Hellman offer their perspectives on the priorities, opportunities, and challenges of patient centricity in real-world evidence collection.
Me, We and RWE. The Importance of Designing for the Patient First
ICON Applies IBM Watson Clinical Trial Matching to Oncology
ICON announced that it is applying IBM's Watson Clinical Trial Matching to its breast, lung, colon and rectal cancer trials.
Certara, Paidion Research Form Pediatric Drug Partnership
Certara® and Paidion Research, announced a new partnership to address the challenges inherent in pediatric drug development.
ACRP Questions Arbitrary CRA Experience
ACRP believes the arbitrary two-years experience generally required throughout the industry is contributing to a shortage of CRAs and negatively impacting efficiencies and quality in clinical research.
CTI Analyzes TB Natural History Database
The analysis compared various manifestations between genotypes and to determine if correlations exist between TSC symptoms and the TSC gene mutation.
Chinese Biopharma Adopts Medidata Cloud in Pediatric Vaccine Program
Medidata, a global provider of cloud-based solutions for clinical research in life sciences, announced that its Clinical Cloud platform has been adopted by Walvax Biotechnology.
Rho Awarded Federal Clinical Services Contract
CRO embarks on the company’s largest-ever federal project.
Almac Expands ‘Direct to Patient’ Service to Europe
Almac announced the expansion of its shipping service for clinical trials to EU countries.
CRO Selects Algorics’ RBM Analytics Solution
The US ophthalmology-focused CRO will use the solution to provide real-time key operational parameters.
BioClinica Announces eHealth App xChange
BioClinica’s eHealth App xChange provides access to an ecosystem of integrated mobile and cloud applications.
PPD Implements Web-based Event Adjudication System
PPD and CISYS LifeSciences announced PPD’s implementation of Sequence WebEAS, a new Web-based event adjudication system, through a collaboration between the two companies.
Kayentis Chooses SFR M2M for Roaming
Kayentis, a French software provider specialized in solutions for clinical trials, has chosen SFR Business Team for its M2M roaming in close to 250 countries.