Why RadPharm
RadPharm is committed to providing the highest quality of service through sound medical, technological and regulatory leadership. This commitment is reflected in RadPharm’s staff – from our senior management team with rich backgrounds in the use of imaging in clinical trials and development of regulatory standards to our large pool of experienced in-house radiologists, nuclear physicians and medical oncologists. We truly are uniquely staffed to focus on the Medicine Behind the ImageTM.
RadPharm couples medical and regulatory expertise with advanced technologies and an experienced project management staff to deliver quality services you can trust to successfully support your drug and device development programs.
When you partner with RadPharm, you are assured:
- Accurate and credible trial data
- Shorter timelines
- Quicker decision-making capabilities
- Regulatory compliance, including 21 CFR Part 11
- Proven, transparent submissions planning and guidance
RadPharm’s expertise has been honed over 16 years, on over 350 studies - Phase I through IV - across 60 countries and spanning all major modalities and therapeutic areas. In addition to having supported more oncology trials than any other imaging core lab, we also possess experience with cardiovascular, musculoskeletal, CNS, diagnostic contrast imaging agents and medical device studies.
Make critical go/no go development decisions faster. Speak to a RadPharm expert today at 877-632-9432 or contact us. |
