Pharmaceutical

Kytes NPD for Pharmaceuticals
and Lifesciences

Solving Pharmaceuticals Challenges with Kytes

Kytes PSA solution is build to solve IT industry challenges.

Evaluating New Product Ideas

Teams lack the acumen to support ideas with strong business cases, use inconsistent methods, and lack standardized metrics, leading to misguided pursuits.

Insufficient Fund Allocation

Without structured business cases, funding decisions lack conviction, negatively impacting financials and weakening competitive strength.

Siloed Project Management

Complex NPD projects suffer from poor integrated planning and execution across teams, leading to, resource allocation, risk management, and lack of focused plan vs. actual measurement.

Imperfect Dossier Management

Lack of comprehensive, structured, and digitized NPD dossiers leads to duplication, inaccuracies, FDA queries, delayed regulatory approvals, and product launch delays.

Disconnected Project Procurement

Unstreamlined procurement processes and poor cost control, causing delays and cost escalation.

Collaboration Across Functions

NPD projects struggle with stakeholder engagement and real-time collaboration, hindered by reliance on spreadsheets, documents, and emails.

Product portfolio visibility and Go-Kill decisions.

IT Projects differ in size, form and complexity. One solution doesn’t fit all and requires fit-to-purpose template and workflows to keep it simple and effective.

Delay in product launches and lost opportunities.

Delays in product launches can lead to missed market opportunities, lost revenue, and reduced competitive edge, impacting overall business growth.

Pharma & Life Sciences Industry Life Cycle

Review the high-level life cycle of IT Projects.

Molecule Approval

  • Molecule Identification
  • Business case development
  • Feedback from CFT
  • Molecule Approval
  • Revenue Forecast

Project Initiation

  • Project Initiation
  • Funding & Budgets
  • Schedule
  • Resource Allocation

Formulation

  • API Procurement
  • Pre-formulation Studies
  • Analytical Method Development
  • Packaging Development
  • Stability Studies

Pilot

  • Batch Size Finalization
  • Pilot Batch Manufacture
  • BE Study

Production & Launch

  • Analytical Method Validation
  • Technology Transfer
  • Manufacture Process Validation Batches
  • Prepare & Submit Dossier
  • FDA Registration
  • Product Launch

Bring clarity, control, and compliance
across every stage of
regulated drug development

Molecule Selection & Business Case Preparation

Evaluates molecule potential and builds quick, data-backed business cases.

Project & Portfolio Management

Provides real-time control over projects, portfolios, and priorities.

Procurement Management

Simplifies vendor selection, purchasing, and material tracking.

Dossier & Document Management

Organizes regulatory documents with accurate, controlled updates.

Launch Management

Coordinates all activities for timely, compliant product launches.

Resource Management

Aligns skills, capacity, and demand for optimal utilization.

Risk
Management

Identifies, tracks, and mitigates risks before they escalate.

Communication & Collaboration

Connects teams with seamless, real-time coordination and information flow.

Benefits

Kytes help you realize your full potential.

Kytes aligns people, processes, and performance for predictable success.

Reduced Time to market icon

Reduced Time to market

30% faster development cycles.

Real time visibility icon

Real-time visibility into product portfolio

25% increase in project accuracy.

Compliance icon

Compliance and first to file

40% reduction in FDA queries and compliance issues.

Improved Productivity icon

Improved Productivity

Building project management culture can create sustainable value in the organization.

Data Consistency icon

Data Consistency

Single version of truth results in 15% reduction in discrepancies.

Our Customers

Customer Testimonials

Resources

Stay Informed. Stay Ahead.