Rapid and University of Florida Awarded $1.65 Million NCI Grant to Enhance Dosimetry Software for Alpha-Emitter Radiopharmaceutical Therapy
Baltimore, Maryland, – Rapid®, in collaboration with Dr. Wesley Bolch and his group
Radiopharmaceutical Imaging and Dosimetry, LLC (Rapid) strives to create a research climate that promotes objectivity in research by establishing standards such that the design, conduct and reporting of Public Health Service (PHS, which includes NIH) funded research is free from bias resulting from financial conflict of interest (FCOI).
Rapid FCOI policy consists of:
1. Policy and procedure: Financial Conflict of Interest in PHS-Funded Projects.
2. Protocol: Protocol for Handling Financial Conflict of Interest.
This policy is applicable to each employee who is planning to or is participating in research activity that is either partially or wholly supported by PHS funds. Each such employee must:
1. Disclose his/her significant financial interests (SFI) in non-Rapid entities that would appear to be related to the employee’s professional responsibilities on behalf of Rapid;
2. Comply with a FCOI management plan, if a FCOI is identified; and 3. Undergo FCOI training, at least once every four years.
Disclosure of SFI is essential for Rapid to determine if a FCOI exists, and in cases of FCOI determine how it will be managed and reported in full compliance with government regulation. Non-disclosure of SFI or non-compliance with FCOI management plan may subject the employee to employment discipline including, without limitation, suspension or termination of employment.
A. Financial conflict of interest (FCOI) means a significant financial interest that could directly and significantly affect the design, conduct, or reporting of PHS funded research.
B. Significant Financial Interest (SFI) exists if the value of remuneration received by the employee, employee’s immediate family (spouse or partner and dependent children) that reasonably appear to be related to the employee’s Rapid responsibilities exceeds $5000; including:
Remuneration received from a publicly traded entity in the twelve months preceding the disclosure and the value of any equity interest in the entity as of the date of disclosure that, when aggregated, exceeds $5,000. For the purposes of this definition, remuneration includes salary and any payment for services not otherwise identified as salary; equity interest includes stock, stock option, or other ownership interest, as determined through reference to public prices or other reasonable measures of fair market value
Remuneration received from a non-publicly traded entity in the twelve months preceding the disclosure that, when aggregated, exceeds $5,000 or any equity interest in such entity.
Intellectual property rights and interests (e.g., patents, copyrights, trademarks) upon receipt of income related to such rights and interests.
Any reimbursed or sponsored travel expenses.
C. Employee’s professional responsibilities on behalf of Rapid means conducting research, submitting patent applications, publication, technical committee membership and, teaching as adjunct faculty at an Institute of higher education.
Baltimore, Maryland, – Rapid®, in collaboration with Dr. Wesley Bolch and his group
Baltimore, Maryland, – Rapid®, a trailblazer in quantitative imaging and dosimetry solutions, is
Baltimore, Maryland – Rapid is pleased to announce that it has received FDA 510(k) market clearance for its first software product: 3D-RD-S, the first web-browser based application that implements the MIRD Schema to perform radiopharmaceutical dosimetry calculations.
We are providing comprehensive expert service and software solutions related to quantitative imaging, dosimetry, in support of pre-clinical and clinical studies needed for regulatory approval.
Radiopharmaceutical Imaging and Dosimetry, LLC (Rapid) is a Baltimore-based company providing comprehensive expert service and software solutions related to quantitative imaging, dosimetry, in support of pre-clinical and clinical studies needed for regulatory approval and for the maximally effective and safe clinical implementation of radiopharmaceuticals.