Practical considerations for navigating the regulatory landscape of non-clinical studies for clinical translation of radiopharmaceuticals

• Main Authors: Aruna Korde (Author), Renata Mikolajczak (Author), Petra Kolenc (Author), Penelope Bouziotis (Author), Hadis Westin (Author), Mette Lauritzen (Author), Michel Koole (Author), Matthias Manfred Herth (Author), Manuel Bardiès (Author), Andre F. Martins (Author), Antonio Paulo (Author), Serge K. Lyashchenko (Author), Sergio Todde (Author), Sangram Nag (Author), Efthimis Lamprou (Author), Antero Abrunhosa (Author), Francesco Giammarile (Author), Clemens Decristoforo (Author)
• Format: Book
• Published: SpringerOpen, 2022-07-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background The development of radiopharmaceuticals requires extensive evaluation before they can be applied in a diagnostic or therapeutic setting in Nuclear Medicine. Chemical, radiochemical, and pharmaceutical parameters must be established and verified to ensure the quality of these nove...