Medical Device Fellowship Program (EEP, OCD, CDRH)
The Center for Devices and Radiological Health (CDRH) Medical Device Fellowship Program (MDFP) provides
opportunities for health professionals to participate in the FDA
regulatory process for medical devices. MDFP is part of External
Expertise and Partnerships (EEP) in the Office of the Center Director in
CDRH. In addition to MDFP, other components of EEP include Technology
Transfer and Partnerships, and the Critical Path Initiative.
CDRH regulates a wide array of medical devices and is involved with
the latest medical device cutting-edge technology areas such as
genomics, proteomics, diagnostics for personalized medicine,
percutaneous heart valves, artificial hearts, tissue engineered wound
dressing with cells, and bone void fillers with growth factors, and many
others.
To keep pace with the rapid development of new technology, and to
make decisions based on the best scientific information and knowledge
available, CDRH routinely consults with experts in the academic
community, other government entities, clinical practice, and the
military. By filling gaps in expertise for a finite period of time, EEP
enhances the efficiency and effectiveness of CDRH operations. EEP is the
focal point of all CDRH fellowships and interorganizational
partnerships. EEP also fosters scientific innovation by helping offices
form partnerships with academia, private sector organizations, and
government agencies.
CDRH established MDFP to increase the range and depth of
collaborations between CDRH and the outside scientific community. The
MDFP offers short and long-term fellowship opportunities for individuals
interested in learning about the regulatory process and sharing their
knowledge and experience with medical devices from the relatively simple
to the highly complex.
Physicians with clinical or surgical expertise, engineers in
biomedical, mechanical, electrical and software areas, and individuals
from many other scientific disciplines have participated in the
fellowship program. Opportunities are available for students in many
areas as well.
Learn about the FDA approval process for medical devices:
- medical device design
- clinical trial design and data
- safety and efficacy evaluation
- materials, performance, bioeffects and standards
- adverse events
Public Service
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- Join CDRH’s mission to protect the public health by ensuring that medical devices are safe and effective
- Share your expertise on complex device issues
- Make a difference in the lives of patients and consumers
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