STRATEGIC BENEFITS FOR CONTRACT RESEARCH ORGANIZATIONS

Helping CROs Win with Workflow Intelligence

Be the CRO Sponsors Count On Every Time

In today’s fast-paced and competitive clinical trial landscape, CROs are under constant pressure to accelerate timelines, maintain strict compliance, and deliver consistent, high-quality results across studies. Our platform simplifies clinical trial process management and boosts collaboration. It replaces complexity with clarity. This helps you reduce risk, enhance visibility, and provide real value to sponsors.

Cloud Concinnity® helps CROs shine as strategic MVPs in every trial phase. Whether it’s managing committees such as DSMBs, CECs (Clinical Events Committees), steering committees, or a range of processes and projects provided by your FSP (functional service provider) unit, they always deliver

“A 50% improvement in administrative tasks demonstrates how Cloud Concinnity® delivers significant business value”

Cloud Concinnity CRO communication access

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

Cloud Concinnity efficiency and speed for CRO

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

Cloud Concinnity mitigate risk for CRO

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

Cloud Concinnity partnerships for CRO

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

Up and Running in Just 30 Days

  • We start by understanding your current processes and workflows. Then, we customize workflow and document templates just for you and confirm integration methods and team roles to ensure a smooth start.

  • Next, we build and set up your study workspace, including dashboards, workflows, and document storage. We also help you add and onboard your users so everyone’s ready to go.

  • Before launch, we walk through your workspace setup, workflows, and security settings together. We finalize the rollout plan to make sure everything meets your needs and compliance standards.

  • Finally, we provide live training and support to your team, assist with user invitations, and help your trial workspace go live. Our goal is to make adoption easy and keep you supported every step of the way

Why Is Cloud Concinnity® the Go-To Partner for CROs

At Cloud Concinnity®, we simplify and standardize clinical trial collaboration across the clinical trial lifecycle, enabling CROs to drive greater value, efficiency, and scalability. Our platform supports every phase from drug discovery to post-marketing, optimizing operations through integrated Program Management, Quality Management, Governance, Risk, and Compliance (GRC), and Product Lifecycle Management

Value-Added Partnerships That Strengthen CRO Success: We help you streamline secure communication across sponsors, committees, and stakeholders. Send regular updates, help teams work together quickly, and automate clinical trial processes. This will ensure transparency, accountability, and real-time oversight throughout your trial.

Add More Value Throughout the Clinical Trial Lifecycle: Stay ahead of clinical trial compliance, improve KPI visibility, and make informed, data-driven decisions without added complexity. Our centralized platform shortens oversight cycles, reduces full-time equivalent (FTE) workload, and makes coordination with committees (DMCs, IRBs (Institutional Review Boards), and CECs (Clinical Events Committees)and FSP project teams effortless.

Enable New Services and Smarter Trial Oversight: Ready to differentiate as a tech-enabled CRO? We help you digitize tasks like contracting, payments, and clinical trial reporting, so you can focus on what drives value. Stay audit-ready with organized documentation and scale new service models with automated workflows built for modern trials.

Expand Capacity Across the Clinical Trial Ecosystem: Support more committees and trial activities without increasing resources. Manage DSMBs, SRCs, and evolving needs with simplicity. This includes interim analyses, publication reviews, and safety monitoring. Our flexible platform adapts to your needs, so you can grow with confidence.