| CPC A61M 5/142 (2013.01) [A61M 5/16831 (2013.01); A61M 5/1785 (2013.01); G16H 10/60 (2018.01); G16H 40/63 (2018.01); A61M 2005/14208 (2013.01); A61M 2005/16863 (2013.01); A61M 2202/0007 (2013.01); A61M 2202/049 (2013.01); A61M 2205/10 (2013.01); A61M 2205/18 (2013.01); A61M 2205/3327 (2013.01); A61M 2205/3331 (2013.01); A61M 2205/3379 (2013.01); A61M 2205/502 (2013.01); A61M 2205/584 (2013.01); A61M 2205/6009 (2013.01)] | 20 Claims |

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1. A radiopharmaceutical drug delivery system comprising;
a configurable dose transporter;
a separable radioactive dose transportation and containment module;
a shielding positioned around at least a portion of the radioactive dose transportation and containment module;
a disposable sealed fluid cartridge mountable within the configurable dose transporter; and
a theranostic informatics management system;
wherein the disposable sealed fluid cartridge comprises:
a) an adapter to secure a drug vial or syringe to the fluid cartridge;
b) one or more integrated fluid channels to allow bi-directional flow of fluids;
c) an integrated precision pump configured to control the flow of a customizable amount of a radioactive drug;
d) a coded patient port and a coded saline port, wherein the coded patient port and the coded saline port are configured to present differently a patient line and a saline line to a user;
e) an integral valve system to control flow of fluids through the integrated fluid channels; and
f) one or more guide features and mechanical interlocks that interact with one or more guide features and mechanical interlocks on the dose transportation and containment module when the fluid cartridge is mounted to the configurable dose transporter.
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