medpace.comDrug and Biologic Contract Research Organization (CRO) | Medpace

Medpace CorporateCareers Investors Investigators Study Participants Blog Japan Site Login Search About Show submenu About Our mission is to accelerate the development of safe and effective medical therapeutics. Company Overview Services & Capabilities Brochure: Trusted by Biotech Read More Whitepaper Winning at Your Drug Development Strategy – A Playbook for Emerging Biotechs Read More Full-Service CRO Trusted by Biotech People. Purpose. Passion. Leadership Global Reach Locations Ethics & Compliance CRO Show submenu CRO Medpace helps biotechs accelerate the development of their medical therapeutics with a full breadth of services and collaborative model. Services Overview Whitepaper A Collaborative Framework for Achieving Diversity, Equity, and Inclusion (DEI) in Clinical Trial Populations Read More Whitepaper Benefits and Challenges of Continuous Glucose Monitoring (CGM) in Clinical Development Read More Study Start-up Clinical Trial Management Show submenu Sites & Patients Patient Diversity in Clinical Trials Decentralized Clinical Trials Clinical Monitoring Clinical Packaging & Supplies Biostats & Data Management Medical Affairs Clinical Safety & Pharmacovigilance Regulatory Affairs & Medical Writing Quality Assurance Technology Therapeutics Show submenu Therapeutics Our therapeutically-focused model gives sponsors early and ongoing insight from medical experts throughout trial design and execution, and facilitates collaboration across specialties to incorporate various medical perspectives and considerations. Our Approach Request Information Blog [Webinar] Unveiling Tomorrow’s Cancer Solutions In an upcoming webinar, Medpace Radiation Oncologist, Jess Guarnaschelli, MD, is joined by TeleDaaS’s Chief Medical Officer, Mark Crockett, MD, and Mirada Medical’s Chief Executive… Read More Webinar Successful Approaches from Rare Disease and Cellular and Gene Therapy Product Approvals Read More Therapeutic Depth Show submenu Cardiovascular Dermatology Endocrine & Metabolic Gastroenterology & Hepatology Hematology & Oncology Immunology & Inflammation Infectious Diseases & Vaccines Nephrology Neuroscience Ophthalmology Crossovers Show submenu Rare Diseases Cell & Gene Therapy Radiation Therapy Women’s Health Pediatrics Medical Device & Diagnostics Labs Show submenu Labs Medpace offers comprehensive and fully-integrated central and bioanalytical laboratory services that deliver efficient and streamlined execution. Integrated for Efficiency Take a Tour Webinar Establishing Efficacy with Flow Cytometry-Based Receptor Occupancy Assays Read More Article The Utility of Liquid Biopsy in Oncology Clinical Trials Read More Central Lab Show submenu Capabilities Biomarkers Safety Testing Featured Methods Therapeutic Expertise Biorepository Services Accreditations Test Directory Bioanalytical Lab Show submenu Capabilities Discovery & Development Preclinical Studies PK Studies TK Studies Biomarker Assays ADA Assays Neutralizing Antibody Assays Bioanalytical Assays & Posters Core Labs Show submenu Core Labs Medpace Core Labs provide an end-to-end suite of global cardiac safety and imaging services to enhance and expedite biopharmaceutical and medical device development. Request Information Blog [Webinar] The Forefront of Radiopharmaceuticals In a recent webinar, Medpace CRO is joined by an emerging biotech to discuss optimal approaches for alpha-RPT clinical trials. Watch now. Read More Webinar Integrating Wearable Remote Biosensor Technology into Decentralized Clinical Trials Read More Imaging Core Lab Show submenu Therapeutic Expertise Show submenu Oncology Imaging Endocrine & Metabolic Imaging MASH/MASLD Imaging Cardiovascular Imaging Neurology Imaging Dermatologic Imaging Nuclear Imaging & Radiopharmaceuticals Musculoskeletal Imaging Image Quantification Services Cardiovascular & ECG Core Lab Wearable Biosensor Technology Phase I Unit Insights Contact Making the Complex Seamless We can’t simplify clinical development – but we can execute it seamlessly Tell us about your upcoming project Quality At Our Core Quality at our core Built to execute – enabled by organic growth Accelerate your clinical development by partnering with a CRO that is structured to keep study teams focused on execution. This commitment to quality extends to the projects we engage in – we are selective to ensure we deliver the highest levels of service and partnering. Our unique approach has been preserved by 30+ years of organic growth – delivering consistency and stability while avoiding the disruptions associated with mergers and acquisitions. Learn More Team Continuity Team Continuity Expertise embedded in trials – throughout the project lifecycle Engage with one cross-functional team that actively participates in your trial or program – from early planning through close-out. Our approach maintains continuity and optimizes performance while building strong team chemistry, minimizing disruptions, and ensuring high-quality results across our full breadth of services. With deep scientific and therapeutic expertise, our teams are poised to lead the industry’s most innovative and challenging clinical trials. Learn More Integrated Services Integrated Services End-to-end partnership – a model of productivity Streamline even the most complex clinical trials with a full-service, single-vendor outsourcing strategy. Our comprehensive CRO services are supported by our wholly-owned Central Laboratories, Bioanalytical Lab, Imaging Core Lab, ECG Core Lab, and Phase I Unit, as well as a Clinical Trial Management System that ties all study data together in a single platform. With integrated services and systems, we achieve higher levels of efficiency and productivity. Learn More Global Engagement GLOBAL Engagement Navigating cultures and requirements – reaching patients around the world Leverage our country-specific experience and breadth of in-house expertise to navigate languages, cultures, and clinical and regulatory environments around the globe. Our resources extend across North America, Europe, Latin America, and Asia Pacific with strong site and Investigator relationships to reach targeted and diverse patient populations. Our global reach and experience across all phases of development and key therapeutic areas can help streamline your clinical trials and reach your development goals faster. 5800 Employees 42 Countries 31 Offices 4 Central Labs Learn More The Medpace Advantage A Full-Service Model for Quality and Efficiency Driven by a full-service CRO model that coordinates and integrates all services for our clients, Medpace provides an accountable, seamless, integrated, and efficient platform for executing clinical research – increasing quality and speed while significantly reducing the need for duplicate management oversight. More than a set of extra hands”, we are an extension of your team – embedding medical, regulatory, and operational expertise into your trials to navigate and overcome challenges. It’s how we make the complex seamless. And it’s why we are Trusted by Biotech ® . Full-Service Model See Why Medpace is Trusted by Biotech Therapeutic Areas Embedded Therapeutic Expertise Medpace employs a high-science and disciplined operating approach that leverages regulatory and therapeutic expertise across all major therapeutic areas. For sponsors, this means your clinical trial will be led by a collaborative team of medical, operational, and regulatory experts with deep knowledge and insights about the disease and the patients your clinical trial is targeting. Backed by over 30 years of experience, our relationships with Key Opinion Leaders, Principal Investigators, and high-performing sites help accelerate clinical development. Explore Our Therapeutic Areas CRO Capabilities Our One Team Approach When you partner with Medpace, you get guidance from our cross-functional team of experts who work together—combining our experience and perspectives—to guide and accelerate your compound through...