Test systems consisting of (a) test kits, (b) detection units, (c) automation units and (d) software for the examination and/or for the detection of biomolecules and/or of active agents from human, animal or vegetable examination materials, with only one parameter or a plurality of parameters being able to be determined at the same time and/or sequentially in a reaction vessel:(a) with the test kit containing the following parts: reaction vessels, such as vials, microtiter plates or filter plates, with the reaction vessels already being able to contain test components in dried form, preferably in freeze-dried form, in predosed form or with the test components being supplied separately as tablet-shaped compacts in vessels, test components consisting of charged carrier particles (encoded particles which are coated with complementary biomolecules/active agents), conjugates (biomolecules and/or active agents marked with one and/or more characteristic marking values), cover films or covers for the closing of the reaction vessels, vessels with suspensions with charged carrier particles (encoded particles which are coated with complementary biomolecules/active agents), vessels with suspensions with test control particles (encoded particles which are coated with the biomolecule/active agent to be detected), vessels with suspensions with detector control particles (encoded particles which are coated with the conjugate or with the characteristic marking values), vessels with diluting buffers, vessels with conjugate (biomolecules and/or active agents which are marked with one and/or more characteristic marking values), vessel with washing buffers (optional), vessel with reconstitution buffers; vessel with recalibration solution(s) (standard); vessel with positive control/negative control/cut-off control, vessel with reference material, vessel with RF absorbent, vessel with stop solution (optional), quality control certificate with nominal values, tolerance ranges and possibilities to quantify the results, working instructions, kit box; (b) with the detection unit comprising: flow cytometer and integrated or external specimen supply station; sheath fluid; flush liquid; cleaning liquid; (c) with the automation unit comprising: barcode module for the positive identification of specimens, controls, reagents and specific kit parameters, specimen receiving module (e.g. specimen carousel, specimen rack), pipetting module (dilution of the specimens, transfer of controls and reagents), transfer module (repositioning of the samples and of the reaction vessels on the work surface), incubation module (shaker unit, optionally temperature settable), optional washing module, pipette tips, waste containers; (d) and with the software comprising: software for the control of the detection unit, software to accept and analyze the data, software for the control of the automation unit, software for the communication between the detection unit and the automation unit, software for the quantitative evaluation and graphical representation of the data.

1) Test systems consisting of (a) test kits, (b) detection units, (c) automation units and (d) software for the examination and/or for the detection of biomolecules and/or of active agents from human, animal or vegetable examination materials, with only one parameter or a plurality of parameters being able to be determined at the same time and/or sequentially in a reaction vessel:(a) with the test kit containing the following parts: reaction vessels, such as vials, microtiter plates or filter plates, with the reaction vessels already being able to contain test components in dried form, preferably in freeze-dried form, in predosed form or with the test components being supplied separately as tablet-shaped compacts in vessels, test components consisting of charged carrier particles (encoded particles which are coated with complementary biomolecules/active agents), conjugates (biomolecules and/or active agents marked with one and/or more characteristic marking values), cover films or covers for the closing of the reaction vessels, vessels with suspensions with charged carrier particles (encoded particles which are coated with complementary biomolecules/active agents), vessels with suspensions with test control particles (encoded particles which are coated with the biomolecule/active agent to be detected), vessels with suspensions with detector control particles (encoded particles which are coated with the conjugate or with the characteristic marking values), vessels with diluting buffers, vessels with conjugate (biomolecules and/or active agents which are marked with one and/or more characteristic marking values), vessel with washing buffers (optional), vessel with reconstitution buffers; vessel with recalibration solution(s) (standard); vessel with positive control / negative control / cut-off control, vessel with reference material, vessel with RF absorbent, vessel with stop solution (optional), quality control certificate with nominal values, tolerance ranges and possibilities to quantify the results, working instructions, kit box;(b) with the detection unit comprising: flow cytometer and integrated or external specimen supply station; sheath fluid; flush liquid; cleaning liquid;(c) with the automation unit comprising: barcode module for the positive identification of specimens, controls, reagents and specific kit parameters, specimen receiving module (e.g. specimen carousel, specimen rack), pipetting module (dilution of the specimens, transfer of controls and reagents), transfer module (repositioning of the samples and of the reaction vessels on the work surface), incubation module (shaker unit, optionally temperature settable), optional washing module, pipette tips, waste containers;(d) and with the software comprising: software for the control of the detection unit, software to accept and analyze the data, software for the control of the automation unit, software for the communication between the detection unit and the automation unit, software for the quantitative evaluation and graphical representation of the data

Test systems consisting of (a) test kits, (b) detection units, (c) automation units and (d) software for the examination and/or for the detection of biomolecules and/or of active agents from human, animal or vegetable examination materials, with only one parameter or a plurality of parameters being able to be determined at the same time and/or sequentially in a reaction vessel:(a) with the test kit containing the following parts: reaction vessels, such as vials, microtiter plates or filter plates, with the reaction vessels already being able to contain test components in dried form, preferably in freeze-dried form, in predosed form or with the test components being supplied separately as tablet-shaped compacts in vessels, test components consisting of charged carrier particles (encoded particles which are coated with complementary biomolecules/active agents), conjugates (biomolecules and/or active agents marked with one and/or more characteristic marking values), cover films or covers for the closing of the reaction vessels, vessels with suspensions with charged carrier particles (encoded particles which are coated with complementary biomolecules/active agents), vessels with suspensions with test control particles (encoded particles which are coated with the biomolecule/active agent to be detected), vessels with suspensions with detector control particles (encoded particles which are coated with the conjugate or with the characteristic marking values), vessels with diluting buffers, vessels with conjugate (biomolecules and/or active agents which are marked with one and/or more characteristic marking values), vessel with washing buffers (optional), vessel with reconstitution buffers; vessel with recalibration solution(s) (standard); vessel with positive control / negative control / cut-off control, vessel with reference material, vessel with RF absorbent, vessel with stop solution (optional), quality control certificate with nominal values, tolerance ranges and possibilities to quantify the results, working instructions, kit box;(b) with the detection unit comprising: flow cytometer and integrated or external specimen supply station; sheath fluid; flush liquid; cleaning liquid;(c) with the automation unit comprising: barcode module for the positive identification of specimens, controls, reagents and specific kit parameters, specimen receiving module (e.g. specimen carousel, specimen rack), pipetting module (dilution of the specimens, transfer of controls and reagents), transfer module (repositioning of the samples and of the reaction vessels on the work surface), incubation module (shaker unit, optionally temperature settable), optional washing module, pipette tips, waste containers;(d) and with the software comprising: software for the control of the detection unit, software to accept and analyze the data, software for the control of the automation unit, software for the communication between the detection unit and the automation unit, software for the quantitative evaluation and graphical representation of the data.