Drug Development and Approval
2014-07-11T20:00:16-04:00https://ximage.c-spanvideo.org/eyJidWNrZXQiOiJwaWN0dXJlcy5jLXNwYW52aWRlby5vcmciLCJrZXkiOiJGaWxlc1wvN2Q0XC8yMDE0MDcxMTA5MTY0MTAwMl9oZC5qcGciLCJlZGl0cyI6eyJyZXNpemUiOnsiZml0IjoiY292ZXIiLCJoZWlnaHQiOjUwNn19fQ==The House Energy and Commerce Subcommittee on Health held a hearing on ways to expedite the Food and Drug Administration’s (FDA) drug development and approval process. Dr. Janet Woodcock, the FDA witness in the first panel, said the agency speeds things up where it safely can but stressed that with some diseases speed was a challenge. Witnesses in the second panel of pharmaceutical and medical organization officials focused on how patients on certain drugs or clinical trials can be beneficial to the drug development and approval process in regard to making the process faster.
The House Energy and Commerce Subcommittee on Health held a hearing on ways to expedite the Food and Drug Administration’s (FDA) drug… read more
The House Energy and Commerce Subcommittee on Health held a hearing on ways to expedite the Food and Drug Administration’s (FDA) drug development and approval process. Dr. Janet Woodcock, the FDA witness in the first panel, said the agency speeds things up where it safely can but stressed that with some diseases speed was a challenge. Witnesses in the second panel of pharmaceutical and medical organization officials focused on how patients on certain drugs or clinical trials can be beneficial to the drug development and approval process in regard to making the process faster. close
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Janet Woodcock M.D. Director U.S. Food and Drug Administration->Center for Drug Evaluation and Research
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