Популярное

Музыка Кино и Анимация Автомобили Животные Спорт Путешествия Игры Юмор

Интересные видео

2025 Сериалы Трейлеры Новости Как сделать Видеоуроки Diy своими руками

Топ запросов

смотреть а4 schoolboy runaway турецкий сериал смотреть мультфильмы эдисон
dTub
Скачать

How does the FDA approve new drugs?

Автор: U.S. Food and Drug Administration

Загружено: 2023-09-06

Просмотров: 72301

Описание:

Prescription drugs go through many steps and phases before they’re approved by the FDA, from research to clinical trials. What does this process look like from beginning to end? Learn more in this short video from FDA’s Center for Drug Evaluation and Research (CDER).

How does the FDA approve new drugs?

Поделиться в:

Доступные форматы для скачивания:

Скачать видео mp4

  • Информация по загрузке:

Скачать аудио mp3

Похожие видео

Investigational New Drug (IND) Submission: Content/Format and First 30 Days (5of14) REdI 2018

Investigational New Drug (IND) Submission: Content/Format and First 30 Days (5of14) REdI 2018

November 13, 2025: Pediatric Advisory Committee Meeting (PAC)

November 13, 2025: Pediatric Advisory Committee Meeting (PAC)

FDA Direct: эти 9 препаратов получили национальные приоритетные ваучеры

FDA Direct: эти 9 препаратов получили национальные приоритетные ваучеры

NDA and BLA Application Review Process (6of15) REdI Annual Conference – May 29-30, 2019

NDA and BLA Application Review Process (6of15) REdI Annual Conference – May 29-30, 2019

Clinical Trial Basics

Clinical Trial Basics

Good Clinical Practice & Pharmacovigilance Compliance Symposium Day Two – PM

Good Clinical Practice & Pharmacovigilance Compliance Symposium Day Two – PM

How FDA Investigates Foodborne Illness Outbreaks

How FDA Investigates Foodborne Illness Outbreaks

FDA’s Regulation of Dietary Supplements with Dr. Cara Welch

FDA’s Regulation of Dietary Supplements with Dr. Cara Welch

FDA Expert Panel on Testosterone Replacement Therapy for Men

FDA Expert Panel on Testosterone Replacement Therapy for Men

Medical Device Quality Management System Regulation Design and Development

Medical Device Quality Management System Regulation Design and Development

Good Clinical Practice & Pharmacovigilance Compliance Symposium | D3S05 - (PV): Future of...

Good Clinical Practice & Pharmacovigilance Compliance Symposium | D3S05 - (PV): Future of...

FDA Direct: An Eye on CDRH: Regulating for a New Era of Medical Devices

FDA Direct: An Eye on CDRH: Regulating for a New Era of Medical Devices

Tobacco Products Scientific Advisory Committee Meeting, October 7, 2025

Tobacco Products Scientific Advisory Committee Meeting, October 7, 2025

The Role of Artificial Intelligence in Clinical Trial Design and Research with Dr. ElZarrad

The Role of Artificial Intelligence in Clinical Trial Design and Research with Dr. ElZarrad

Components of New Drug Application and Biologics License Application (5of15) REdI– May 29-30, 2019

Components of New Drug Application and Biologics License Application (5of15) REdI– May 29-30, 2019

Medical Device Quality Management System Regulation Risk Management

Medical Device Quality Management System Regulation Risk Management

FDA Direct: Removing Black Box Warnings for HRT (Part 1/2)

FDA Direct: Removing Black Box Warnings for HRT (Part 1/2)

Importing FDA-Regulated Products: The Import Process

Importing FDA-Regulated Products: The Import Process

GCP & Pharmacovigilance Compliance Symposium | D3S03-1 - (BE): Clinical Study Conduct

GCP & Pharmacovigilance Compliance Symposium | D3S03-1 - (BE): Clinical Study Conduct

FDA Direct: Catching Up on Agency Reforms

FDA Direct: Catching Up on Agency Reforms

© 2025 dtub. Все права защищены.



  • Контакты
  • О нас
  • Политика конфиденциальности



Контакты для правообладателей: [email protected]