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How Ideas2IT Built an Oncology Guidelines Platform for a F500 Pharmaceutical Leader

How Ideas2IT Built an Oncology Guidelines Platform for a F500 Pharmaceutical Leader

Table of Contents

Addressing challenges in oncology care

With the increasing volume of clinical research and oncology treatment guidelines, healthcare professionals face challenges in accessing and interpreting the most up-to-date, relevant clinical guidelines for their patients. Multiple guidelines exist for the treatment of various types of cancer, and these can be difficult to navigate, particularly when trying to integrate them into the workflow of a busy healthcare environment. The need for accurate, current, and easily accessible guidelines is critical, especially as oncology treatments and practices continue to evolve.

Furthermore, healthcare institutions may have unique treatment pathways that differ from national or international standards, necessitating the ability to customize and display these pathways to ensure consistency in care delivery across the organization.

Building a unified oncology guidelines solution

In tackling the technical complexities of oncology care, we focused on creating a seamless and comprehensive solution that enhanced both the user experience and treatment outcomes.

  • A platform designed to integrate the latest NCCN guidelines to align with the healthcare organization’s unique practices.
  • The solution presented clinical guidelines in a digital flowchart format, providing clinicians with a clear, interactive path for each treatment option, improving accessibility and understanding.
  • Clinicians could now easily search for and retrieve relevant treatment protocols through a streamlined query system, ensuring they had access to the latest, most accurate guidelines.
  • By linking each guideline to its source, clinicians were empowered to independently review and verify the information, increasing transparency and trust in the guidelines.

The application is explicitly designed to support healthcare professionals in their decision-making but is not intended to replace professional judgment or be used as a primary diagnostic tool.

Outcomes of Implementing a Unified Oncology Guidelines Solution

The Oncology Guidelines application was implemented across multiple healthcare institutions and integrated into existing hospital information systems. The application was accessible through web-based platforms, with mobile support for on-the-go usage. The time spent by clinicians searching for relevant treatment protocols was reduced by 60%, significantly improving workflow efficiency.

  • Increased Access to Guidelines: Healthcare professionals now have immediate access to a comprehensive library of oncology guidelines, helping them stay up to date with the latest treatment recommendations without the need for manual searches across multiple resources.
  • Enhanced Decision-Making: The flowchart interface allowed for easier navigation of complex treatment protocols, enabling faster decision-making and more consistent care delivery.
  • Customization Adoption: Institutions adopted the customization features, ensuring that treatment pathways were aligned with their organizational standards while still incorporating nationally and internationally recognized guidelines.
  • Streamlined Workflows: Integration with existing systems streamlined workflows, reducing time spent searching for guidelines and allowing healthcare professionals to focus more on patient care.

By combining the latest oncology treatment guidelines with customized institutional pathways, Ideas2IT successfully empowered healthcare providers to enhance clinical decision-making, streamline workflows, and improve patient care outcomes. 

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Case Study

How Ideas2IT Built an Oncology Guidelines Platform for a F500 Pharmaceutical Leader

How Ideas2IT Built an Oncology Guidelines Platform for a F500 Pharmaceutical Leader

Solutions Deployed:

  • Oncology Guidelines Application
  • Digital Flowchart Presentation

Vertical:

Pharma & Life Sciences

Addressing challenges in oncology care

With the increasing volume of clinical research and oncology treatment guidelines, healthcare professionals face challenges in accessing and interpreting the most up-to-date, relevant clinical guidelines for their patients. Multiple guidelines exist for the treatment of various types of cancer, and these can be difficult to navigate, particularly when trying to integrate them into the workflow of a busy healthcare environment. The need for accurate, current, and easily accessible guidelines is critical, especially as oncology treatments and practices continue to evolve.

Furthermore, healthcare institutions may have unique treatment pathways that differ from national or international standards, necessitating the ability to customize and display these pathways to ensure consistency in care delivery across the organization.

Building a unified oncology guidelines solution

In tackling the technical complexities of oncology care, we focused on creating a seamless and comprehensive solution that enhanced both the user experience and treatment outcomes.

  • A platform designed to integrate the latest NCCN guidelines to align with the healthcare organization’s unique practices.
  • The solution presented clinical guidelines in a digital flowchart format, providing clinicians with a clear, interactive path for each treatment option, improving accessibility and understanding.
  • Clinicians could now easily search for and retrieve relevant treatment protocols through a streamlined query system, ensuring they had access to the latest, most accurate guidelines.
  • By linking each guideline to its source, clinicians were empowered to independently review and verify the information, increasing transparency and trust in the guidelines.

The application is explicitly designed to support healthcare professionals in their decision-making but is not intended to replace professional judgment or be used as a primary diagnostic tool.

Outcomes of Implementing a Unified Oncology Guidelines Solution

The Oncology Guidelines application was implemented across multiple healthcare institutions and integrated into existing hospital information systems. The application was accessible through web-based platforms, with mobile support for on-the-go usage. The time spent by clinicians searching for relevant treatment protocols was reduced by 60%, significantly improving workflow efficiency.

  • Increased Access to Guidelines: Healthcare professionals now have immediate access to a comprehensive library of oncology guidelines, helping them stay up to date with the latest treatment recommendations without the need for manual searches across multiple resources.
  • Enhanced Decision-Making: The flowchart interface allowed for easier navigation of complex treatment protocols, enabling faster decision-making and more consistent care delivery.
  • Customization Adoption: Institutions adopted the customization features, ensuring that treatment pathways were aligned with their organizational standards while still incorporating nationally and internationally recognized guidelines.
  • Streamlined Workflows: Integration with existing systems streamlined workflows, reducing time spent searching for guidelines and allowing healthcare professionals to focus more on patient care.

By combining the latest oncology treatment guidelines with customized institutional pathways, Ideas2IT successfully empowered healthcare providers to enhance clinical decision-making, streamline workflows, and improve patient care outcomes. 

Case Study

How Ideas2IT Built an Oncology Guidelines Platform for a F500 Pharmaceutical Leader

How Ideas2IT Built an Oncology Guidelines Platform for a F500 Pharmaceutical Leader

Solutions Deployed:

  • Oncology Guidelines Application
  • Digital Flowchart Presentation

Vertical:

Pharma & Life Sciences

Addressing challenges in oncology care

With the increasing volume of clinical research and oncology treatment guidelines, healthcare professionals face challenges in accessing and interpreting the most up-to-date, relevant clinical guidelines for their patients. Multiple guidelines exist for the treatment of various types of cancer, and these can be difficult to navigate, particularly when trying to integrate them into the workflow of a busy healthcare environment. The need for accurate, current, and easily accessible guidelines is critical, especially as oncology treatments and practices continue to evolve.

Furthermore, healthcare institutions may have unique treatment pathways that differ from national or international standards, necessitating the ability to customize and display these pathways to ensure consistency in care delivery across the organization.

Building a unified oncology guidelines solution

In tackling the technical complexities of oncology care, we focused on creating a seamless and comprehensive solution that enhanced both the user experience and treatment outcomes.

  • A platform designed to integrate the latest NCCN guidelines to align with the healthcare organization’s unique practices.
  • The solution presented clinical guidelines in a digital flowchart format, providing clinicians with a clear, interactive path for each treatment option, improving accessibility and understanding.
  • Clinicians could now easily search for and retrieve relevant treatment protocols through a streamlined query system, ensuring they had access to the latest, most accurate guidelines.
  • By linking each guideline to its source, clinicians were empowered to independently review and verify the information, increasing transparency and trust in the guidelines.

The application is explicitly designed to support healthcare professionals in their decision-making but is not intended to replace professional judgment or be used as a primary diagnostic tool.

Outcomes of Implementing a Unified Oncology Guidelines Solution

The Oncology Guidelines application was implemented across multiple healthcare institutions and integrated into existing hospital information systems. The application was accessible through web-based platforms, with mobile support for on-the-go usage. The time spent by clinicians searching for relevant treatment protocols was reduced by 60%, significantly improving workflow efficiency.

  • Increased Access to Guidelines: Healthcare professionals now have immediate access to a comprehensive library of oncology guidelines, helping them stay up to date with the latest treatment recommendations without the need for manual searches across multiple resources.
  • Enhanced Decision-Making: The flowchart interface allowed for easier navigation of complex treatment protocols, enabling faster decision-making and more consistent care delivery.
  • Customization Adoption: Institutions adopted the customization features, ensuring that treatment pathways were aligned with their organizational standards while still incorporating nationally and internationally recognized guidelines.
  • Streamlined Workflows: Integration with existing systems streamlined workflows, reducing time spent searching for guidelines and allowing healthcare professionals to focus more on patient care.

By combining the latest oncology treatment guidelines with customized institutional pathways, Ideas2IT successfully empowered healthcare providers to enhance clinical decision-making, streamline workflows, and improve patient care outcomes. 

Connect with Us

We'd love to brainstorm your priority tech initiatives and contribute to the best outcomes.

From Data Errors to Regulatory Confidence: A Case Study in Clinical Trial Data Integrity and AI Compliance

One-liner summary:
Ideas2IT built an AI-powered data integrity platform for a global pharmaceutical company, eliminating clinical trial data errors, standardizing outputs to CDISC SDTM, and accelerating regulatory readiness.

The Problem with the Status Quo

Clinical trial data must be accurate, complete, and compliant. This pharmaceutical leader faced increasing pressure from regulatory bodies due to inconsistencies, missing data, and unflagged anomalies that delayed approvals and increased audit risk.

Manual cleanup and spreadsheet workflows could not keep up with the volume or complexity of modern trials. Issues surfaced late during audits or submission prep, causing delays, rework, and revenue loss.

Where the Gaps Were

Key challenges included:

  • Discrepancies between EDCs, CRFs, and patient registries
  • Missing data due to input errors, site variability, or subject dropout
  • Undetected anomalies that surfaced only during audits
  • Manual QA cycles that consumed analyst time and delayed regulatory submissions
  • Lack of CDISC SDTM standardization, leading to friction during FDA and EMA reviews

A scalable solution was needed to surface and resolve these issues earlier in the process.

What We Delivered

Ideas2IT designed and deployed a modular AI platform to detect, resolve, and standardize clinical trial data in real time fully aligned with regulatory expectations.

Core Components:

  • Inconsistency Detection Engine
    AI models cross-referenced clinical data across systems, historical patterns, and protocol benchmarks to identify mismatches and route them for review.
  • Missing Data Recovery
    Statistical and contextual inference models flagged missing values and suggested imputation paths, enabling dataset completion without compromising integrity.
  • Anomaly Detection
    Models surfaced outliers, unexpected trends, and protocol deviations across patient cohorts and trial timelines.
  • CDISC SDTM Standardization
    All corrected outputs were structured according to CDISC SDTM, enabling smoother submissions to FDA, EMA, and other global regulators.
  • Deployment Architecture
    Containerized, API-accessible services hosted on AWS, ready to scale across trials and trial phases.

The platform moved quality assurance upstream making data integrity part of the trial pipeline, not a post-hoc fix.

Outcomes We Achieved

Capability Impact
Data review cycles Shortened through automated detection and correction
Submission readiness Improved with CDISC SDTM-aligned outputs
Regulatory compliance Strengthened with traceable corrections and audit logs
Approval timelines Accelerated by reducing remediation loops
Analyst productivity Increased through reduction in manual QA effort

The client can now submit clinical trial data with higher confidence and lower friction resulting in faster regulatory approvals and greater operational efficiency.

Industry
Pharma & Life Sciences
Location
USA
Tech Stacks
Challenge

Oncology clinicians struggled to find and apply the right treatment guidelines amid a flood of evolving protocols and fragmented documentation. Customization across institutions added more complexity.

Key Takeaways

  • Manual QA won’t scale. Real-time AI validation reduces bottlenecks and regulatory exposure
  • Transparent imputation matters. Predicted values must be flagged and traceable
  • CDISC SDTM should be embedded. Compliance must be native to the pipeline
  • Clean data builds trust. Regulators move faster when the data is consistent, reviewable, and audit-ready

Co-create with Ideas2IT

We show up early, listen hard, and figure out how to move the needle. If that’s the kind of partner you’re looking for, we should talk.
We’ll align on what you're solving for - AI, software, cloud, or legacy systems
You'll get perspective from someone who’s shipped it before
If there’s a fit, we move fast — workshop, pilot, or a real build plan
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