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急上昇中の質問
Driving Site Activation
Accelerating site activation can jumpstart a clinical trial, but with the hours and weeks spent manually tracking tasks and documents without visibility into where the bottlenecks lie, how can you make that happen?
Activate Cloud Service enables sponsors, CROs, and sites to get studies started in the shortest time possible. Activate workflows drive study teams to complete and track specific documents and tasks required for any site, country, or study based on regulatory and SOP requirements.
Activate Cloud Service Benefits
- Improve operational performance with 70+ smart, standardized country workflows for quick study activation
- Automatically trigger workflows and alert study team members when prerequisite work is complete
- Ensure appropriate activity access with role-based assignments and retain knowledge even through staff turnovers
- Guide compliance with organizational SOPs and country-specific regulations
- Streamline document management by sharing study documents from a centralized library
- Deliver transparency with real-time study progress reporting and risk mitigation
- Enhance planning with predictive capabilities that guide team members in milestone planning activities
- Utilize multi-plan comparison and visualization tools to scenario plan optimal study setup
Oracle Health Sciences end-to-end study startup solution stood out for the opportunity it provides us to eliminate traditional bottlenecks in the flow of clinical data, which can impact study quality and lead to unnecessary delays.
Study Startup Webcasts
COVID-19's Impact on the Digital Transformation of Clinical Trials
Learn how digital transformation roadmaps were accelerated to embrace innovative approaches to overcome adversary.
Are the Intended Benefits of ICH Regulations Obscured by the Adoption Struggle?
Learn how fundamental to new ICH guidelines is the modernization of processes and technology with a focus on QbD and risk-based management approaches.
Using Artificial Intelligence to Improve Clinical Trial Efficiency and Optimization
Learn how machine learning technologies can help predict outcomes in clinical trials, leading to faster drug approval times and lower costs.
Outsourcing to CROs: Expediting Clinical Operations or Oversight Nightmare?
Learn how to overcome the complexities introduced in outsourced studies (e.g., quality, oversight, collaboration, and governance).
Dismantling Data Silos to Improve Study Startup and Mitigate Risk
Learn how entrenched silos have stymied data flow efforts due to minimal understanding of what is needed downstream.
Avoid Rescue Studies, Reduce Costs and Timelines, and Accelerate Clinical Operations with Metrics
Drive competitive performance and operational excellence by focusing on bottlenecks and processes ripe for optimization.
Ensuring Quality and Risk Mitigation with Proactive Planning in Clinical Trials
Learn how good clinical practice (GCP) guidelines and systems help improve overall study quality.
The Importance of Contemporariness and an Approach to Mitigate Audit Findings
Learn how contemporariness can be defined in operational SOPs and implemented in daily operations to ensure audit readiness.
Standardization Drives Transparency and Optimization in Clinical Trial Startup
Learn how to tackle the challenge of improving budget and contract cycle times in starting clinical trials.
Refocusing on Risk Mitigation in Starting Clinical Trials
Discover how to combat poor risk management practices that have fueled the rescue study industry.
Is Site-Centric Engagement Paramount to Clinical Trial Success?
Hear how eClinical technologies and industry initiatives are impacting the ability of investigative sites to conduct clinical trials.
Will Decentralized Clinical Trials Compound Patient and Data Quality Risks?
Learn how to mitigate the patient and data quality risks associated with decentralized clinical trials.
News and Resources
Clinical trials are constantly evolving, with advancements in technology, industry initiatives, and regulatory, and process changes. Gain perspective and learn more about these changes in the resources below.
Activate’s robust, industry proven library of country-specific workflows and management-based approach to site activation is central to our efforts to build out our infrastructure of ‘best of breed’ applications in our eClinical suite.
What's New in Study Startup
White Papers
- Don't Settle for Less: Redefining the Core and Scope of Study Startup
- Analytics and Metrics Help Pinpoint Costs of Study Startup
- Breathing Life into SOPs with an Automated Workflow-Driven Process
- Moving Beyond Excel to Purpose-Built Applications for Speedier Study Startup
- Building Risk Assessment and Mitigation into Study Startup
- Study Startup Solutions Improve CRO Oversight Through Collaboration
- Study Startup: New Battleground in CRO Differentiation Strategy
- Spotlight on Quality in Study Startup
Research Reports
- ChromoReport Spring 2020 - Importance of Leading Indicators to Machine Learning Predictive Models (PDF)
- ChromoReport Winter 2019 - Proactive Planning with Predictive Analytics
- ChromoReport Fall 2019 - Performance of Multi-Country vs. Single Country Studies
- Impact Assessment of eClinical Technologies and Industry Initiatives on Sites
- ChromoReport Summer 2019 - Utilizing a Risk-Based Approach to Contract Optimization
- eClinical Technology Adoption and Challenges in Study Startup
- Tufts CSDD START II Site Selection
- Tufts CSDD Assessing Practices and Inefficiencies
- Tufts CSDD START Study Initiation Cycle Times