Strategic Benefits of Cloud Concinnity for Contract Research Organizations
Purpose built for clinical trial oversight, Cloud Concinnity centralizes, simplifies and automates crucial information, processes and tracking that significantly impact the course of a program. Integrated across the eClinical ecosystem, Cloud Concinnity securely coordinates data from disparate systems for more controlled, well-informed and auditable decision making. Improved collaboration, reporting, meeting management and communication, within and across studies, create strategic benefits for CROs and their customers.
IMPROVE INFORMATION ACCESS, CONTROL & SECURITY
All participants have direct, easy access to what they need, when they need it
Individual and role-based permissions ensure appropriate access
Integrated platform eliminates data leakage/loss through email & other point solutions
Integration creates a single source of truth for decision making and reporting
Comprehensive solution eliminates security holes not addressed by other solutions
INCREASE PROCESS EFFICIENCY, SPEED & PROFITABILITY
Turn SOPs into Workflows to ensure productivity, compliance and accountability
Configurable & re-usable workflows speed implementation
Monitor information and activities both within & across programs
Identify and address process inefficiencies, inconsistencies & workload imbalances
Live document editing, e-signatures & videoconferencing save time & money
All aspects of meeting management coordinated/automated through one system
MITIGATE RISK ACROSS THE ECOSYSTEM
Centralizing multiple streams of information saves time & reduces errors
Automating processes (SOPs) ensures consistency, quality & compliance
Controlled document retention and future access deliver only what’s required
Role-based access allows for easier migration of responsibilities during transitions
CREATE STRONGER, VALUE-ADDED PARTNERSHIPS
Collaborate & communicate appropriately, easily and securely with Sponsors/Committees
Provide timely, standardized communications to Sponsors & Executive Management
Program compliance, KPI tracking, improved study/product lifecycle decision making
Add more value by reducing trial oversight cycle time and/or FTE effort
Differentiate as a provider of repeatable, scalable, tech-enabled solutions
Enable new services replacing cumbersome manual processes, i.e. contracting, payments
Expand capacity to serve multiple participants/activities in clinical trial oversight ecosystem
EOCs, DMCs, DSMBs, SRCs, Ad Boards
Adaptive Trial Designs, Publication Review, Interim Analysis, PV