TY - JOUR
T1 - Guideline on current good radiopharmacy practice (cGRPP) for the small-scale preparation of radiopharmaceuticals
AU - Gillings, Nic
AU - Hjelstuen, Olaug
AU - Ballinger, Jim
AU - Behe, Martin
AU - Decristoforo, Clemens
AU - Elsinga, Philip
AU - Ferrari, Valentina
AU - Peitl, Petra Kolenc
AU - Koziorowski, Jacek
AU - Laverman, Peter
AU - Mindt, Thomas L
AU - Neels, Oliver
AU - Ocak, Meltem
AU - Patt, Marianne
AU - Todde, Sergio
PY - 2021/2/12
Y1 - 2021/2/12
N2 - This guideline on current good radiopharmacy practice (cGRPP) for small-scale preparation of radiopharmaceuticals represents the view of the Radiopharmacy Committee of the European Association of Nuclear Medicine (EANM). The guideline is laid out in the format of the EU Good Manufacturing Practice (GMP) guidelines as defined in EudraLex volume 4. It is intended for non-commercial sites such as hospital radiopharmacies, nuclear medicine departments, research PET centres and in general any healthcare establishments. In the first section, general aspects which are applicable to all levels of operations are discussed. The second section discusses the preparation of small-scale radiopharmaceuticals (SSRP) using licensed generators and kits. Finally, the third section goes into the more complex preparation of SSRP from non-licensed starting materials, often requiring a purification step and sterile filtration. The intention is that the guideline will assist radiopharmacies in the preparation of diagnostic and therapeutic SSRP's safe for human administration.
AB - This guideline on current good radiopharmacy practice (cGRPP) for small-scale preparation of radiopharmaceuticals represents the view of the Radiopharmacy Committee of the European Association of Nuclear Medicine (EANM). The guideline is laid out in the format of the EU Good Manufacturing Practice (GMP) guidelines as defined in EudraLex volume 4. It is intended for non-commercial sites such as hospital radiopharmacies, nuclear medicine departments, research PET centres and in general any healthcare establishments. In the first section, general aspects which are applicable to all levels of operations are discussed. The second section discusses the preparation of small-scale radiopharmaceuticals (SSRP) using licensed generators and kits. Finally, the third section goes into the more complex preparation of SSRP from non-licensed starting materials, often requiring a purification step and sterile filtration. The intention is that the guideline will assist radiopharmacies in the preparation of diagnostic and therapeutic SSRP's safe for human administration.
UR - http://www.scopus.com/inward/record.url?scp=85102603114&partnerID=8YFLogxK
U2 - 10.1186/s41181-021-00123-2
DO - 10.1186/s41181-021-00123-2
M3 - Journal article
C2 - 33580358
SN - 2365-421X
VL - 6
SP - 8
JO - EJNMMI radiopharmacy and chemistry
JF - EJNMMI radiopharmacy and chemistry
IS - 1
M1 - 8
ER -