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One Team - One Approach

Our full breadth of services and collaborative model provide the ideal platform to execute studies at the highest level of quality.

Our full breadth of services and collaborative model provide the ideal platform to execute studies at the highest level of quality.

Study Strategy

  • Medical
  • Operations
  • Regulatory Affairs
  • Biometrics
  • Clinical Informatics & Feasibility
  • Labs
  • Imaging
Optimize your development strategy with insights and guidance from experts across Medpace.

Study Execution

  • Regulatory Services
  • Study Start-Up
  • Clinical Trial Management
  • Vendor Management
  • Clinical Packaging & Supplies
  • Patient Recruitment & Retention
  • Clinical Monitoring
  • Data Management
  • Biostatistics
  • Medical Monitoring
  • Safety & Pharmacovigilance
  • Endpoint Adjudication
  • Independent Data Monitoring Committee (IMDCI)
  • Medical Writing
  • Quality Assurance
  • Account Management

Integrated Services

  • Central Labs
  • Bioanalytical Labs
  • Imaging Core Labs
  • Cardiovascular Labs
  • Phase I Unit
Even the most complex study designs are streamlined by working with a single vendor with the expertise and staffing needed to collect and analyze critical endpoints.

Technology

  • Clinical Trial Management System
  • Electronic Data Capture (EDC)
  • ePRO / eCOA / eDiary / eConsent
  • Interactive Response Technology (IRT)
  • ClinTrak Data Explorer
  • Centralized Monitoring
  • eTMF
  • Wearables
  • Imaging Management
  • TrialPACE Patient App
  • OnPACE Site App
  • Lab Information
  • Management System (LIMS)
Abstract Network Background

Streamline your development

We offer a full partnership instead of an “extra set of hands.” Our full breadth of services and collaborative model provide the ideal platform to execute studies at the highest level of quality.

Helping You Push the Boundaries of Clinical Research

Biotech innovation is transforming the world. In parallel,  clinical development is increasingly more complex  and challenging – from scientific, operational and regulatory perspectives. We help biotechs – the trailblazers of the industry – accelerate the development of their therapeutic under our full-service model that  combines operational, medical, and regulatory expertise with our own wholly owned labs, imaging services, cardiac safety, and Phase I Unit, to provide our clients with one integrated solution.

Comprehensive Services and Capabilities

In the complex environment of clinical development, the more vendor partners that are involved, the higher the chance for conflicts in the drug development process. This is where our full-service model with comprehensive services streamlines the process and – Makes the Complex Seamless for our Sponsors. Competence and empowerment to coordinate all services under one roof provides an accountable, integrated, and efficient platform – increasing quality and speed while significantly reducing a Sponsor’s need for duplicate management oversight. From First-In-Human studies through late phase clinical development, we provide comprehensive services and capabilities to support your studies and programs.

Doctor watching herpatient sign paperwork

female scientist writing on a whiteboard

Right-sized for Responsiveness

Biotechs are confronted with an ever-changing slate of top priorities. The ability to fully rely on your CRO to execute studies – almost independently – allows you to focus on other pressing issues. Being Trusted by Biotech® means that we form collaborative relationships and our teams are as invested in the science of your products as much as you are. At the same time, we are large enough to conduct complex trials globally, yet small enough to maintain a higher level of commitment.