Life Sciences and Pharma

Drive faster trials, approval cycles and manage risk

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Skan for Life Sciences and Pharma

Join leading life sciences and pharma organizations using Skan’s AI-powered Process Intelligence to streamline workflows through standardization and automation, improve quality and compliance by reducing rework and SLA violations, and enhance productivity through training and by eliminating non-value added activities.

Plane

Drive Operational Excellence

Identify standardization and automation opportunities to boost productivity, and reduce variability, processing time and turnaround time.

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Improve Quality & Compliance

Continuously monitor processes to identify opportunities to reduce errors and rework, as well as reduce service level agreement (SLA) violations.  Proactively manage risk with real-time alerts linked to leading indicators of quality and compliance.  

Three Color Start

Enhance Productivity

Improve time and efficiency across the board, from procurement to clinical trial initiation by reducing manual reworks & speeding up cycle time

Skan for life sciences and pharma

Skan for Life Sciences and
Pharma

Leading life sciences and pharma organizations use process intelligence across critical business operations and use cases.

Research and Development (R&D)

Research and Development (R&D)

Optimize drug discovery, and regulatory submission workflows 

  • Drug Discovery Workflow
  • Clinical Trial Planning and Design
  • Preclinical Testing and Validation
  • Regulatory Submissions Preparation
  • Collaboration in Research Teams

Clinical Trials Management

Clinical Trials Management

Drive operational excellence in patient enrollment, data monitoring and adverse event reporting.

  • Patient Recruitment and Enrollment
  • Study Protocol Adherence
  • Data Collection and Monitoring
  • Site Management and Coordination
  • Adverse Event Reporting

Regulatory Compliance and Submissions

Regulatory Compliance and Submissions

Reduce errors, rework, and SLA breaches.

  • Regulatory Document Preparation
  • Submission Planning
  • Quality Control and Assurance for Submissions
  • Regulatory Authorities Management
  • Post-Approval Compliance Monitoring

Quality Management and Assurance

Quality Management and Assurance

Enhance efficiency, reduce errors, and meet quality assurance goals

  • Deviation and Non-Conformance Management
  • Corrective and Preventive Actions (CAPA)
  • Change Control Management
  • Audit Management
  • Document Control and Management

Research and Development (R&D)

Optimize drug discovery, and regulatory submission workflows 

Business Use Cases
  • Drug Discovery Workflow
  • Clinical Trial Planning and Design
  • Preclinical Testing and Validation
  • Regulatory Submissions Preparation
  • Collaboration in Research Teams

Clinical Trials Management

Drive operational excellence in patient enrollment, data monitoring and adverse event reporting.

Business Use Cases
  • Patient Recruitment and Enrollment
  • Study Protocol Adherence
  • Data Collection and Monitoring
  • Site Management and Coordination
  • Adverse Event Reporting

Regulatory Compliance and Submissions

Reduce errors, rework, and SLA breaches.

Business Use Cases
  • Regulatory Document Preparation
  • Submission Planning
  • Quality Control and Assurance for Submissions
  • Regulatory Authorities Management
  • Post-Approval Compliance Monitoring

Quality Management and Assurance

Enhance efficiency, reduce errors, and meet quality assurance goals

Business Use Cases
  • Deviation and Non-Conformance Management
  • Corrective and Preventive Actions (CAPA)
  • Change Control Management
  • Audit Management
  • Document Control and Management

Business Value Metrics

Leading life sciences and pharma organizations use Skan to drive better business outcomes and compliance

30 %

Process turnaround timereduction

F500 Lifesciences organization

20 %

Production volume increase

Leading Lifesciences Payer

25 %

Error rate reduction

Global Pharma leader

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