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Use of a rare disease patient registry in long-term post-authorisation drug studies

Use of a rare disease patient registry in long-term post-authorisation drug studies

FromThe Lancet Respiratory Medicine in conversation with


Use of a rare disease patient registry in long-term post-authorisation drug studies

FromThe Lancet Respiratory Medicine in conversation with

ratings:
Length:
9 minutes
Released:
May 5, 2018
Format:
Podcast episode

Description

Dr. Diana Bilton joins The Lancet Respiratory Medicine to discuss how the use of rare disease patient registries helps with long term drug studies after drug authorisation.
Released:
May 5, 2018
Format:
Podcast episode

Titles in the series (100)

Editors speak to the journal’s authors to explore their research and its impact on people’s health, health care, and health policy in this regular podcast.