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Therapeutically focused clinical research organization - CRO - Medpace
Therapeutically Specialized Clinical Research

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Find out how our medical, regulatory, and operational expertise in clinical development can help with your next study or program.

Experts, Experience and Execution to
Streamline and Accelerate your Clinical Trials

Medpace is your trusted advisor for the entire clinical development process. We deliver strategic therapeutic leadership from planning through every phase of your project. Medpace expertise and focus brings three key advantages to our Sponsors: 

  • In-depth therapeutic knowledge: Led by some of the industry’s most distinguished medical experts/scientists, Medpace brings valuable insights and knowledge to your research-based drug development. This expertise can significantly speed your pathways to commercialization.
  • Extensive Phase I-IV experience across therapeutic specialties: With Phase I-IV experience in multiple therapeutic specialties around the globe, Medpace is able to leverage our therapeutic experience to provide greater efficiencies, and better designed and executed studies.
  • Global regulatory leadership: Medpace regulatory experts − former government officials with valuable insight to the specific areas of drug approval – work to ensure that every phase of trial is correctly focused and designed for regulatory approval.

Areas of Therapeutic Expertise

 By focusing in select therapeutic fields, Medpace is able to collaborate more effectively with all stakeholders and ultimately accelerate your drug towards approval. Our growing list of therapeutic specialties includes:
  • Cardiology: Medpace has vast experience in both drug and device cardiovascular trials, as well as the conduct of large cardiovascular endpoint trials.
  • Central Nervous System: Drugs for neurologic disorders are increasingly critical for the well-being of the world. Medpace is a leader in helping Sponsors speed the commercialization of new therapies.
  • Infectious Disease and Vaccines: Responding to the global demand for anti-infectives, Medpace has compiled a team of therapeutic and regulatory experts to assist in streamlining drug approval.
  • Endocrine - Metabolic Disorders: Medpace has extensive experience in trial design, drug classes, and disease endpoints for Phase I-IV research in this area. Medpace's experience in conducting diabetes trials around the world is unmatched by any other Clinical Research Organization (CRO).
  • Nephrology: Medpace understands the full spectrum of renal disease and has access to these difficult-to-find patients.
  • Oncology: Medpace responds to the urgent need to develop new oncologic therapies with a dedicated team of oncology specialists who understand the unique complexities of oncology trials.
  • Regenerative Medicine holds the bold promise of discovering new therapeutic approaches to combat diseases that are still out of reach of traditional drugs and biologicals.
  • Gastrointestinal Medpace offers medical leadership in GI, as well as other areas that may cross over into GI studies including infectious disease, metabolic/diabetes, and oncology, as well as the Medpace Imaging Core Lab for central imaging.

September 5 - 9, 2014
Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC)
Washington, US

September 13 - 17, 2014
Transcatheter Cardiovascular Therapeutics (TCT)
Washington, US

September 14 - 17, 2014
18th Annual Scientific Meeting of the HFSA
Las Vegas, US

15 - 19 September 2014
50th EASD Annual Meeting
Vienna, AT

26 - 30 September 2014
ESMO 2014 Congress
Madrid, ES

October 7 - 8, 2014
Stem Cell Meeting on the Mesa
La Jolla, US

7 - 11 October 2014
World Muscle Society Congress
Berlin, DE

October 8 - 12, 2014
Philadelphia, US

October 11 - 14, 2014
American Academy of Pediatrics Experience
San Diego, US

October 18 - 22, 2014
UEG Week
Vienna, AT


request info Medpace is ready to help you with your next clinical trial project. Find out more about how we can help.

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