Insights On Clinical Technologies
92% Accuracy In Early Parkinson’s Classification
Academic researchers and two biopharma leaders teamed up with Clinical ink in the WATCH-PD Study to test the power of at-home mobile devices to assess Parkinson’s Disease progression. The work, described here, is an important step in seeking regulators’ qualification of novel digital assessments in early Parkinson’s Disease.
The EU (536/2014) CTIS Database Has Been Approved – What Happens Now?
In January 2022, EU (536/2014) – a binding regulation across all members of the EU – came into effect. The new regulation will streamline procedures and remove duplication of single submission via a single EU portal. It also focuses on an assessment procedure leading to a single decision, rules on the protection of subjects and informed consent, a greater level of harmonization, and transparency requirements.
The Case For A Clinical Data Strategy
Many life sciences companies are looking for ways to transform their approach to become data driven organizations with digital health initiatives. Explore why this requires an organizational approach and vision around data strategy.
Digital Outcome Measures Approved As Primary Endpoint In Cardiopulmonary Study
Discover how a clinical development program was saved using objective, continuous digital outcome measures.
Achieving Better Healthcare Outcomes: A Leap Forward In Safety
Watch as panelists delve into the value of real-world data (RWD) and real-world evidence (RWE) to safety programs, how applications and data work together, impacts on post-marketing safety and adverse event monitoring, and innovative ideas for future success.
Machine Learning And KOL Networks: The Future Of Medical Affairs
New technology is offering a way for medical affairs teams to stay on top of changing patterns and improve focus on building mutually beneficial relationships with key opinion leaders.
Award-Winning Solution Solves Big Pain Point For Clinical Trials
Learn how the built technology was able to eliminate expenses and errors associated with the manual abstraction of electronic health record data into clinical trial research databases, and case report forms.
Enhancing Oncology Clinical Trials Through The Use Of Digital Technologies
The most difficult clinical research just became more challenging. Receive tactics on how teams can simplify oncology research while solving new and old issues.
Industry-First eTMF AI: PhlexTMF v21
PhlexTMF v21 is pre-trained on millions of documents and embeds the cumulative guidance of hundreds of Phlexglobal’s TMF experts. The result? More clinical documents are “right-first-time” at document upload, helping prevent document misfiles and metadata errors before they occur - and reducing queries and time-consuming remediation.
The Future Of Clinical Data Management: The Intersection Of Data Management And Clinical Operations
Today there are instances where more than 70% of clinical trial data points are not collected via eCRFs. Now, data management teams are evaluating approaches from clinical operations such as risk-based quality management to increase focus on critical data. Listen to this exciting discussion from industry experts as they bring data management and clinical operations together.