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Capabilities

Experts in all phases of clinical development phase I to IV. Contact us today to see how Solace can accelerate your next trial.

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At Solace Clinical Research, we offer a comprehensive suite of capabilities to support your clinical research needs. With a strong commitment to advancing medical science, we are equipped to handle studies across all phases, from early-phase trials to complex, high-volume studies.
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Specialized in Phase 1

Our Phase 1 capabilities are designed to accelerate drug development by providing early insights into the safety, pharmacokinetics, and dosing of investigational products.

Solace’s state-of-the-art facilities and experienced team are dedicated to delivering comprehensive data and ensuring a seamless transition from preclinical research to human trials. We specialize in pioneering early-phase research, setting the foundation for the success of later-phase studies.

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Therapeutic expertise

We are proud to offer expertise across multiple therapeutic areas, ensuring precision and specialized knowledge in each study we conduct. 

Our key areas include:

Cardiology

Pain Management

Neurology

Endocrinology

Infectious diseases

Vaccinology

Rheumatology

Nephrology

State-of-the-art facilities

Our facilities are fully equipped to handle complex trials, offering an environment that supports the rigorous demands of clinical research. We ensure every site adheres to the highest standards of safety.

  • CLIA-certified laboratories
  • IATA-certified staff
  • GCP-trained physicians
  • Class IIA BSC
  • Onsite PBMC
  • Advanced data management systems
  • 24/7 emergency patient hotline
  • Refrigerated and -70°C freezers
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Clinical trial management

From Phase I to Phase IV, Solace provides comprehensive clinical trial management, ensuring efficiency, compliance, and the highest standards of data accuracy.

Regulatory affairs

Expert guidance through complex regulatory requirements to expedite approvals and ensure compliance.

Patient recruitment & retention

Proven strategies to engage diverse patient populations, ensuring high-quality data and successful study outcomes.

Data management & analysis

Advanced systems to manage and analyze trial data, providing real-time insights and ensuring actionable results.

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Integrated Operations for Rapid Site Selection

Our streamlined operations ensure quick and efficient site activation, tailored to your study’s needs:
  • Fast Turnaround Times: Contracts and budgets are reviewed and returned within 48 hours.
  • Unified Agreement: A single contract simplifies collaboration across all our sites.
  • Centralized Communication: A dedicated point of contact ensures smooth coordination throughout the process.
  • Extensive Network: With 30+ sites and over 190 investigators, we offer a comprehensive and simplified site assessment process.
  • Tech-Driven Forecasting: Advanced tools provide precise enrollment projections based on your study’s protocol.

Streamlined Start-Up Processes

We accelerate study start-up through standardized procedures and advanced technology:
  • Quick Launch: From award to initiation visit in 30 days or less.
  • On-Site Laboratory Capabilities: Select locations feature PBMC processing and labs to enhance efficiency.
  • Integrated Technology: Tools for stipends, eReg, EMR/EHR, and same-day shipping make processes seamless.
  • Expert Training: Site staff receive tailored start-up training to ensure readiness.
  • Dedicated Support: Every study is assigned a clinical data specialist for optimal management.
  • Centralized Collaboration: We align with your preferred central IRB or laboratory for smooth integration.

Exceptional Patient Engagement and Retention

Our strategies focus on recruiting and retaining participants while promoting diversity and inclusion:
  • Comprehensive Databases: Access to proprietary physician and practice networks for faster enrollment.
  • Immediate Support: Recruitment efforts begin as soon as the study starts.
  • Community-Centered Outreach: Programs tailored to engage diverse populations and promote inclusivity.
  • In-House Advertising: Custom campaigns outperform traditional centralized approaches.
  • Retention Programs: Initiatives to maintain participant adherence and long-term engagement.
  • Specialized Facilities: Niche care sites provide access to unique patient populations and specialized procedures.

Commitment to Quality and Accurate Data

We deliver reliable data with a steadfast commitment to quality at every stage:
  • Rapid Data Management: Data entered within 48 hours and queries resolved promptly.
  • Quality Assurance Checks: Routine and random reviews, including cross-checks between EDC and source documents.
  • Ongoing Training: Regular education for investigators and site staff to ensure excellence.
  • Certified Expertise: Our labs are CLIA-certified, and all staff are trained in GCP and IATA standards.

SOLACE CLINICAL RESEARCH

Why choose Solace?

Experienced team

Our team is comprised of seasoned professionals with extensive experience in clinical research, patient care, and regulatory compliance.

Patient-centric approach

We prioritize patient safety and comfort, maintaining ethical standards and high-quality care throughout the trial process.

Innovative solutions

We leverage cutting-edge technology and methodologies to enhance trial efficiency, accuracy, and outcomes.

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