33
/es/
AIzaSyAYiBZKx7MnpbEhh9jyipgxe19OcubqV5w
August 1, 2025
7975116
757069
2
Public Timelines
Public TimelinesFAQ
Public TimelinesFAQ
For educational institutions For teachers For students Cabinet
For educational institutions For teachers For students Open cabinet
Crear
Create a timeline
Public timelines
Library
FAQ

1 ene 2007 año - Food and Drug Administration Amendments Act of 2007

Descripción:

Specifically authorized FDA to require manufacturers post-marketing clinical studies to monitor for risks infected during the pre-market approval process
Also required REMS programs where necessary. What is a REMS program?

Añadido al timeline:

Pharmacy Law Timeline

ByRachel Collins
21 feb 2023
0
0
222

fecha:

1 ene 2007 año
Ahora mismo
~ 18 years ago
About & FeedbackAcuerdoPrivacidadBibliotecaFAQ
Support 24/7  
CabinetGet premium
Donate
The service accepts bank transfer (ACH, Wire) or cards (Visa, MasterCard, etc). Processed by Stripe.
Secured with SSL