How European Oncology Site Networks Streamline Clinical Trial Site Selection
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Deliver your oncology therapy at scale with a CRO built to streamline development for personalized medicines. World-class teams and technologies, broad capabilities, and deep oncology expertise will support you from promising molecule to patient impact.
(Within the past 3 years)
As an oncology contract research organization, we excel at running complex trials such as basket and umbrella trials with adaptive design, master protocols with multiple treatment cohorts, and biomarker-driven trials with intricate sample collection. Our team of clinical trial design experts is ready to assist on your next trial.
With pioneering experience and integrated services, we support the entire lifecycle of cell and gene therapies. Partner with the leader in clinical development, manufacturing, and commercialization to bring your groundbreaking treatments to market.
Biomarker use in Oncology clinical trials for the industry is now over 55% of all studies. Biomarker validation is critical to your drug and clinical program’s success. Delivering new biomarker tests to support clinical trials and personalized therapy is our passion. Work with the leaders in biomarker development and validation at Precision for Medicine.
Oncology expertise in Biomarker Development including:
Developing a companion diagnostic for your clinical program? Precision for Medicine has over 15 years of experience as an oncology CRO in guiding sponsors down the companion diagnostic pathway.
We leverage established technologies, proprietary approaches, and develop and validate biomarker assays to generate robust biomarker data in samples ranging from nucleic acids to tissues
Biomarkers & Specialty Lab ServicesTissue
Cell
Protein
RNA
DNA
Are you planning a companion diagnostic? Precision’s Companion Diagnostics team can guide
and support your development, regulatory, and commercialization journey. The route to market for a companion
diagnostic is complex and must be well planned to ensure that the test and drug come to market together,
with the best possible patient access.
Relationships with the oncology investigator community matter, as selecting the right sites can predetermine many factors, from on-time enrollment to high-quality data.
Precision invests heavily in building these relationships to make the right sites available to our partners' studies.
Global Oncology Centers
Access preidentified and prequalified centers from around the world with extensive infrastructures, expertise, and most importantly, access to the patient populations you need for your trials.
Ensure consistent site adherence and data-driven decision-making throughout your trial. Precision Centralized Monitoring bridges the gaps in standard data review processes with integrated oncology research standards, such as RECIST, RECIST 1.1, and CTCAE.
The team’s extensive oncology expertise guarantees a comprehensive examination of data against specific standards, maintaining the integrity of your dataset.
Leverage tools like JReview Cloud, SAS, and Precision’s Smart Patient Profiles to enhance data visualizations, making remote reviews more efficient and insightful.
Experiences, tips, and perspectives from experts on the front lines of research.
All ResourcesLeverage an integrated infrastructure that reduces the inefficiencies inherent in complex development. Integrate lab and trial execution to increase speed to market. Incorporate manufacturing expertise for advances therapies to ensure scalability. Precision can customize and converge our capabilities for your program's unique needs.
Award-winning CRO with deep oncology and rare disease expertise
Exceptional translational and biomarker sciences with global central lab services
Pioneers in planning, building and maintaining manufacturing at scale for pharma and biotechs.