Pharmaceuticals & biotechnology

Clinical Trial Site Feasibility & Activation

Coordinates clinical trial site feasibility, investigator credentials and facility readiness.

Request a tailored demonstration Explore the interface

13 workspace menus · 5 role profiles · Connected records

Designed for programme coordinators and the responsible business owners

Clinical Trial Site Feasibility & Activation workspace interface preview; illustrative records and figures. — **Clinical Trial Site Feasibility & Activation — operational workspace**Interface preview · Illustrative dataView full interface →

Explore the system interface.

Operational workspace and record review. Select a screen to inspect it in full.

Clinical Trial Site Feasibility & Activation record interface preview; illustrative records and figures. — **Clinical Trial Site Feasibility & Activation — record and workflow review**Interface preview · Illustrative dataView full interface →

Operational dashboards and work queues.

Operational views

Review work, evidence, exceptions and authorised decisions within a defined operating scope.

Site / programmePeriodAssigned teamReview state

Dashboard measures

Active planning proposals
Count of all records in the selected workspace.
Review queue
Records at the third stage of the business workflow.
Needs attention
Records with an assigned review requirement.
Final-stage records
Records in the fourth business workflow stage.

Business workflow and operating scope

Coordinates clinical trial site feasibility, investigator credentials and facility readiness. Tracks contracts, required approvals and unresolved activation tasks, then records authorised site opening and handover, with a complete evidence trail supporting each readiness decision.

Operational visibility

Workload and progress by site / programme
Outstanding reviews and assigned actions
Evidence completeness and exception history
Accepted outcomes and follow-up obligations

Operations

Operational overview

Review the work position and priority actions.

Clinical trial site feasibility

Coordinate clinical trial site feasibility with assigned responsibilities, linked records and review history.

Investigator credentials

Coordinate investigator credentials with assigned responsibilities, linked records and review history.

Facility readiness

Coordinate facility readiness with assigned responsibilities, linked records and review history.

Contracts

Coordinate contracts with assigned responsibilities, linked records and review history.

Approvals

Coordinate approvals with assigned responsibilities, linked records and review history.

Unresolved activation tasks

Coordinate unresolved activation tasks with assigned responsibilities, linked records and review history.

Site opening

Coordinate site opening with assigned responsibilities, linked records and review history.

Handover

Coordinate handover with assigned responsibilities, linked records and review history.

Insights

Reports and saved views

Review the reporting scope and export agreed operational views.

Governance

Approvals and exceptions

Review delegated decisions, exceptions and recorded conditions.

Audit history

Trace accepted changes, decisions and accountable actions.

Access and configuration

Manage the agreed role permissions and configurable operating rules.

The end-to-end business journey.

From intake to authorised completion, with evidence at each decision.

Capture the proposal

Establish the scope of clinical trial site feasibility, capture the required records and assign the accountable team.

Compare scope and assumptions

Coordinate investigator credentials and facility readiness with linked evidence and visible outstanding actions.

Approve the allocation

Review the relevant conditions and exceptions. Record the authorised outcome and its supporting evidence.

Track revisions and commitments

Confirm the resulting records and handovers. Track remaining obligations, later changes and follow-up actions.

Governance and control

Role permissions reflect the agreed responsibilities and restricted record access.
Required information and evidence are checked before the relevant decision or handover.
Exceptions have a named owner, recorded reason and an authorised resolution.
Approved changes retain their previous values, accountable decisions and linked evidence.
Integration mappings, business rules and acceptance criteria are reviewed with the customer.

Accountable roles

Programme coordinator

Quality specialist

Evidence reviewer

Authorised release reviewer

Platform administrator

Permissions are configured and tested for the agreed responsibilities.

Data, interfaces and operating requirements.

Core records

Planning proposalClinical trial site feasibilityInvestigator credentialsFacility readinessContractsApprovalsDecisionSupporting evidenceActivity history

Systems and interfaces

Quality and controlled document records
Laboratory, trial or product information interfaces
Identity and role-based access services
Approved document and communication services

Interface scope, data mapping and testing are agreed for each engagement.

Implementation requirements
Confirm the operating boundaries for clinical trial site feasibility, responsible roles, review authority, record retention, interface mappings and acceptance scenarios.

Mobile and tablet access

Authorised users can review clinical trial site feasibility, supporting records and assigned actions through mobile and tablet access. The relevant tasks and permissions are agreed for the deployment.

Access approved workflows through the Dalfin mobile app. Device tasks and permissions are confirmed for the deployment.

Apple App Store ↗Google Play ↗

AI extensions

Core workflows and approval rules are defined with your business owners. Operational AI can be assessed separately against a specific business outcome and review requirements.

AI extensions are scoped around the required data, business outcome and review controls.

Engineered with Genesis.

Structured application engineering

Connect requirements, roles, records, workflows and interfaces through the agreed Genesis engineering process.

Controlled changes

Review dependency impact and validation requirements. Context Memory supports governed changes and accepted application revisions.

Deployment and support

Agree customer cloud or on-premises requirements, device access, implementation acceptance and ongoing engineering support.

Explore the platform

Genesis architecture →

Context Memory →

An example operating scenario

See the process, its exception and the evidence.

Start with clinical trial site feasibility and follow the record through the ‘Compare scope and assumptions’ stage. Introduce a missing item or operating exception, record the authorised resolution and inspect the final handover, evidence and history.

What to review

A saved end-to-end transaction
An exception and its authorised resolution
Different operator, approver and reviewer permissions
Final records, history and the relevant report

Discuss this solution

Questions before implementation.

What can we review in a tailored demonstration?

Review a representative planning proposal, its workflow stages, accountable roles, an exception and the resulting operational report. Bring the business process and existing system requirements that matter to your organisation.

How is the solution adapted to our organisation?

The operating scope covers your records, role permissions, review authority, business rules and integration boundaries. These requirements are agreed with the responsible business owners.

How does the solution connect with existing systems?

Connection design defines interfaces, data ownership, mapping, authentication and exception handling. The agreed implementation includes validation against the selected systems and workflows.

How are subsequent changes controlled?

The agreed engineering approach covers review of change impact, bounded implementation, validation and accepted revisions. Discuss the relevant Genesis Context Memory and support requirements during solution scoping.