GMP production in full compliance with pharma industry standards of quality and confidentiality and in compliance with ICH Q7 (GMP for APIs), chapter 19 (APIs for use in clinical trials)
Establishing DMF (Drug Master File) for PET and SPECT precursors
Performance of stability studies
Custom research, consultancy service and expertises for the production of new or already existing/known PET precursors for the execution of clinical and pharmaceutical studies/trials.