Background: There are only a handful of true theranostic matched pairs, and in particular the theranostic radiocopper trio ⁶¹Cu, ⁶⁴Cu and ⁶⁷Cu, for diagnosis and therapy respectively, is a very attractive candidate. In fact, the alternative of two imaging radionuclides with different half-lives is a clear advantage over other theranostic pairs, since it offers a better matching for the tracer biological and radionuclide physical half-lives. Due to the high availability of ⁶⁴Cu, its translation into the clinic is being successfully carried out, giving the example of the FDA approved radiopharmaceutical Detectnet (copper Cu 64 dotatate injection). However, a shorter-lived PET radionuclide such as ⁶¹Cu may as well be beneficial. Results: Proton irradiation of enriched ⁶²Ni electrodeposited targets with a compact cyclotron produced the desired radionuclide via the ⁶²Ni(p,2n)⁶¹Cu nuclear reaction, leading to ⁶¹Cu activities of up to 20 GBq at end of bombardment and 8 GBq at end of purification. Furthermore, two purification methods are compared leading to comparable results regarding separation yield and product purity. Following the radiochemical separation, quality assessment of this product [⁶¹Cu]CuCl₂ solution proved radionuclidic purities (RNP) over 99.6% and apparent molar activities (AMA) of 260 GBq/µmol with the 1,4,8,11-tetraazacyclotetradecane-1,4,8,11-tetraacetic acid (TETA) chelator, end of purification corrected. Conclusions: In the current article a comprehensive novel production method for the PET radionuclide ⁶¹Cu is presented, providing an alternative to the most popular production routes. Characterization of the [⁶¹Cu]CuCl₂ product showed both high RNP as well as high AMA, proving that the produced activity presented high quality regarding radiolabeling up to 9 h after end of purification. Furthermore, production scalability could be easily achieved by increasing the irradiation time. Graphical abstract: [Figure not available: see fulltext.]