Experience a better clinical trial experience for all stakeholders while bringing new treatments to market faster.

Clinical Functional Service Provider (FSP) solutions are ideal for addressing gaps in services or clinical development programs, while allowing Clients to maintain control over operations and data. FSP partners enable organizations to quickly adapt to changing priorities and challenges, injecting agility and facilitating cost and efficiency gains while enabling access to critical site relationships. Solutions range from small scale supplementation to end-to-end development of complete clinical programs to support centralized or decentralized efforts.

Clinical Support Capabilities available across all Therapeutic Areas:

    • Real World Evidence (RWE) / Real World Data (RWD)
    • Feasibility Assessment
    • Site Identification & Selection
    • Protocol Development
    • Study Startup
    • Rescue Studies
    • Site Engagement
    • Patient Recruitment
    • eTMF & Document Management
    • Clinical Monitoring
    • Medical Monitoring
    • Pharmacovigilance / Drug Safety
    • Supply Chain Management
    • Therapeutic Area Expertise
scientist holding a model

Managed by seasoned industry experts and protected by DOD-level security, IPS is equipped to design and manage truly secure clinical programs specific to each project’s requirements. We will identify, hire, train and manage the right team of qualified Project Leaders, Client Delivery Directors and Clinical Research Associates, enabling easy access to senior experts and clinical resources from across the organization. Whether centralized, decentralized, or hybrid, rest assured knowing your projects are fully staffed with the precise skillsets required for successful program execution.

These guiding principles support our gold standard of a customized, agile, and cost-effective approach to clinical trial development. Combined with unwavering commitment to each program, our clients reap the rewards of a superior clinical trial experience for all stakeholders, while bringing new treatments to market faster.

  • DOD level data security to protect your IP
  • Meticulous data management and statistical analysis
  • Trusted collaboration and proactive communication
  • Robust quality control measures
  • Rigorous management of site activity
  • Dedicated specialist resources ensure programs stay on-time and on-budget
  • Specific therapeutic area expertise
  • Agility to quickly adapt to changes in study design or protocols
  • Centralization / Decentralization capabilities
  • Real-time data access integrated with your organization's software systems