MCHRI Drug & Device Development Training Program
CURRICULUM
The D3 training program curriculum will be centered around the hands-on involvement on a medical product development project currently in the clinical phase within one of the program’s industry partners. Opportunities to individualize training and topics covered will be determined by the awardee and include interacting with different functional areas such as:
Medical Development
Clinical Pharmacology
Regulatory Affairs
Clinical Operations
Biostatistical
Bioanalysis
Chemistry and Manufacturing
Technology
Preclinical DMPK,
Pharmacology & Toxicology
In addition, self-directed learning through curated readings and online webinars from the NIH and FDA on various aspects of medical product development will be available. Participation in already established programs and courses relevant to this training program within the Stanford community before and after the onsite industry experience will also be valuable to supplement and enrich the training experience. Development of a personalized program curriculum will be generated by a Stanford faculty member after acceptance into the program.
For questions about the program, please contact Grant Wells.