Act on clinical trials of medicinal products for human use - scope of regulation and sources of law
The development of pharmaceutical sciences results in the development of many new medicinal products that require thorough examination of their safety and effectiveness in the course of clinical trials before obtaining marketing authorization. Post-war ethical and legal regulations for conducting cl...
Saved in:
Main Author: | Małgorzata Maria Kubacka (Author) |
---|---|
Format: | Book |
Published: |
Polish Pharmaceutical Society,
2024-02-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Regulation (EU) No 536/2014 on clinical trials on medicinal products for human use: an overview
by: Carlo Petrini
Published: (2014) -
Polish legal pharmaceutical market regulations since 1918
by: Małgorzata Maria Kubacka
Published: (2020) -
Reforming the Regulation of Therapeutic Products in Canada: The Protecting of Canadians from Unsafe Drugs Act (Vanessa's Law)
by: Katherine Fierlbeck
Published: (2016) -
Reforming the Regulation of Therapeutic Products in Canada: The Protecting of Canadians from Unsafe Drugs Act (Vanessa's Law)
by: Katherine Fierlbeck
Published: (2016) -
THE INTERPRETATION OF DIVINE WILL AS THE SOURCE OF JEWISH LAW IN THE CONTEXT OF THE POTENTIAL OF HUMAN'S FREEDOM OF WILL
by: hieromonk Dmytro (Frankiv)
Published: (2020)