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Biopharma Regulatory Requirements with bluebird bio's Scott Cleve

Biopharma Regulatory Requirements with bluebird bio's Scott Cleve

FromBusiness Of Biotech


Biopharma Regulatory Requirements with bluebird bio's Scott Cleve

FromBusiness Of Biotech

ratings:
Length:
40 minutes
Released:
Apr 26, 2021
Format:
Podcast episode

Description

Scott Cleve brings an entire career dedicated to the mastery of global biopharma regulatory standards to his role as Vice President of Regulatory Operations and Compliance at bluebird bio. Join Cleve, host Matt Pillar, and Erin Harris, chief editor at Cell & Gene, for a candid discussion on the regulatory trends shaping the advance of bluebird's pipeline of gene therapies for the treatment of serious, life-altering diseases including Cerebral Adrenoleukodystrophy, Multiple Myeloma, Transfusion-Dependent β-Thalassemia, and Sickle Cell Disease.
Released:
Apr 26, 2021
Format:
Podcast episode

Titles in the series (100)

The Business of Biotech is the pod dedicated to leaders of emerging biopharma firms. We bring you insight into organizational, finance and funding, HR, clinical, manufacturing, and regulatory challenges you’ll face as you navigate your company from an idea to success in the clinic. Each episode features guest commentary and best practices from accomplished founders and biopharma industry luminaries. The Business of Biotech is produced by BioProcess Online and brought to you by Cytiva, formerly GE Healthcare Life Sciences.