Corporate Overview
RadPharm is a leading full service imaging core lab, managing all facets of the imaging segment of global clinical trials, Phases I-IV. We employ board-certified, sub-specialty trained radiologists, nuclear physicians and oncologists to focus on “The Medicine Behind the Image™” and deliver medical expertise, advanced technology and a proven operational process - thereby assuring accurate, timely trial data and successful regulatory submissions.
About RadPharm
Founded on medical expertise and a commitment to quality and service excellence, RadPharm has facilitated clinical drug development by streamlining the image acquisition process through the application of proactive, technological solutions. Our global service offerings include Charter Development, Image Acquisition/ Tracking & Management, Image Interpretation & Clinical Assessment, Regulatory Guidance, Medical Physics Support, Site Qualification and Consulting Services.
Mission Statement:
To be the leading provider of integrated state-of-the-art imaging technologies and services facilitating successful new drug development.
At a glance, we offer...
- Unprecedented clinical trial experience in +60 countries and over 5,000 unique sites around the world
- On-staff, board-certified radiologists, oncologists and nuclear physicists
- 'Fast-Track' regulatory approval due to exemplary trial preparedness
- A proven track record of exceptional service, quality and innovation
- Experienced project teams working to comprehensive communications plans
- Dedicated 24/7/365 site support
- Innovative technologies that are continually enhanced and refined to meet the evolving needs of the industry
- Flexibility to meet timelines and deliverables in a quality environment
- Regulatory compliance, including 21 CFR part 11
RadPharm provides centralized, independent, blinded interpretation of medical imaging for clinical studies and a proven planning, tracking and implementation process from protocol design through regulatory submission.
RadPharm imaging services are performed in a stringent quality environment, ensuring GCP and 21 CFR part 11 compliance.
All Major Modalities:
- Angiography
- Computed Tomography (CT)
- Magnetic Resonance Imaging (MRI)
- Nuclear Medicine
- Positron Emission Tomography (PET)
- PET/CT
- Medical Photography
- Single Photon Emission Computed Tomography (SPECT)
- Ultrasound
- X-Ray
Our Services:
Image Interpretation
- By board-certified, sub-specialty trained RadPharm staff radiologists
- Eligibility, efficacy and safety read scenarios
Imaging Process
- Study initiation and start up
- Site initiation and 24/7 support
- Image acquisition, tracking and management
- Data management
Clinical Assessments
- Medical photography
- Oncology clinical data review
- Radiation therapy QA
Molecular Imaging
- Quantitative and qualitative physiological response measurements
- Site qualification
- Medical physicist support
Regulatory
- Charter development
- Proven submission planning and process
- Experienced regulatory guidance, including in-person consultation
- Image repository and documentation database design and delivery
- Image storage and archiving
Global Experience
Supporting the global clinical trial industry since 1993, our vast expertise spans early stage clinical through phase IV studies in all major therapeutic areas. In addition to having supported more oncology trials than any other core lab, we also possess deep experience with cardiovascular, musculoskeletal, CNS, diagnostic contrast imaging agents and medical device studies.
Headquartered in Princeton NJ, RadPharm also has an office located in Munich, Germany.
Our People
RadPharm understands that our success is the result of our experienced staff - Our people are the difference. From project onset, a Project Manager is assigned to provide a single point of contact throughout the life of a study. An experienced project team, including a sub-specialty trained radiologist, will collaborate to develop and implement a streamlined process based on your study protocol, driven by a comprehensive communication plan. Our board-certified staff physicians, along with the other project team members, are readily accessible to discuss the project and answer any queries.
RadPharm’s team of professionals are recognized industry physicians, innovators and technology experts, many are regularly invited to be key-note speakers at industry conferences and authored prominent industry publications. Our highly-regarded staff will be instrumental in your study’s overall success.
RadPharm is committed to providing the highest quality of service through proven medical, technological and regulatory leadership. |
