A History of Success. We are a Contract Research Organization (CRO)
implementing Risk-Based Management through the use of
Quality by Design (QbD) methodologies, which helps
accelerate a study and reduces overall risk.
Phase I Phase II-III Phase IV Medical Devices & DIagnostics Audits
A History of Success. Start from the ground-up...
evaluate the situation from high above... from a vantage point,
then ground yourself and plan, implement, verify and execute.
Phase I Phase II-III Phase IV Medical Devices & DIagnostics Audits

    Vantage BioTrials Inc. is a privately-held, Contract Research Organization (CRO) that provides Phase I-IV clinical trial management services to international pharmaceutical, biotechnology, generic pharmaceutical and medical device companies.


    Vantage BioTrials has become a leader in providing clinical trial management services by implementing Quality by Design (QbD) strategies, Risk-Based Approaches to Monitoring and process improvement methods to the entire clinical trial lifespan.


    Vantage BioTrials’ level of quality service has been a distinguishing factor over the years as we are continually challenging ourselves to achieve goals beyond our ability.  As proof, we’ve had the honor of being the recipient of several notable awards and accomplished numerous milestones.

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Prioritizing Agility When Choosing a Contract Research Organization
Publication date: September 2023 / Download PDFAuthor: Josée Comeau Introduction Throughout the years, the field of clinical research has continued to grow in complexity and has encountered numerous challenges, and although processes have been well established, many of us have settled into a daily routine that maintains the status quo. It’s time for us to… Read more
Perfectly on Time: Successfully Managing Clinical Trial Deliverables
Publication date: November 2022 / Download PDFAuthors: Vatche Bartekian, Johanna Garcia, Sheila Ernest Introduction A key skill for clinical Project Managers (PM) within the life sciences industry is time management. As a PM, you are not only responsible for the project deliverables, but for every person involved as well as every task performed. Yes, it… Read more
Planning a Positive Outcome for Your Clinical Trial
Publication date: September 2022 / Download PDFAuthor: Vatche BartekianCo-Authors: Johanna Garcia, Kaiser Lagman, Marina Ohouo,Sheila Ernest Introduction The drug development process presents many complex steps and requires a keen set of skills, knowledge, and resources to arrive successfully at subsequent stages . Within the various phases of drug development, clinical trials, in particular, require robust,… Read more