IVD Devel­op­ment

Our val­ue propo­si­tion: Qual­i­ty & Inno­va­tion

With our research & devel­op­ment depart­ment we con­tribute to the devel­op­ment of high-qual­i­ty in-vit­ro diag­nos­tics and sup­port our part­ners with prod­ucts and qual­i­fied exper­tise.

Cross-plat­form test sys­tems & con­trols

We devel­op in-vit­ro diag­nos­tics (IVD) in form of test sys­tems and con­trols with CE mark­ing. Our work is plat­form-inde­pen­dent, com­pris­ing ELISA kits, rapid tests, and auto­mat­ed sys­tems.

In addi­tion to our own devel­op­ments, we coop­er­ate with part­ners from sci­ence and phar­ma­ceu­ti­cal & diag­nos­tic indus­try in both fields, human and vet­eri­nary.

For us, the qual­i­ty of a devel­op­ment is sub­stan­tial­ly defined by the qual­i­ty of the used sam­ples which is reflect­ed in our com­pe­tence in the field of pro­vid­ing human biospec­i­mens.

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From Autoim­mu­ni­ty to Oncol­o­gy

Our coop­er­a­tion with Diag­nos­tikNet BB enables us to han­dle the com­plete IVD prod­uct cycle from fea­si­bil­i­ty study to CE-marked.

There­fore, we could already real­ize numer­ous projects which are applied in rou­tine diag­nos­tics as well as in ther­a­py deci­sions, e.g. autoim­mune dis­eases, the deter­mi­na­tion of small mol­e­cules, and mon­i­tor­ing in the field of nov­el food / nutri­tion­als.

EQAS & Kit Exter­nal Con­trols

On the one hand, we sup­port many Euro­pean EQAS providers with con­trols in order to ensure inter-lab­o­ra­to­ry qual­i­ty con­trol, while on the oth­er hand, we offer the devel­op­ment and pro­duc­tion of kit-exter­nal and man­u­fac­tur­er-inde­pen­dent con­trols for the use in lab­o­ra­to­ry rou­tine.

Immunoas­says – From PoC to Auto­mat­ed Sys­tems

In the field of test sys­tems we are espe­cial­ly focused on immunoas­says. These dif­fer, for exam­ple, from chem­i­cal reac­tion meth­ods such as the Jaf­fé reac­tion for the detec­tion of cre­a­ti­nine or the mea­sure­ment of the ery­thro­cyte sed­i­men­ta­tion rate.

A typ­i­cal rep­re­sen­ta­tive of immunoas­says is the ELISA (Enzyme-linked Immunosor­bent Assay) which usu­al­ly con­sists of two anti­bod­ies that bind an anti­gen in the sam­ple by form­ing a sand­wich com­plex and enabling its quan­tifi­ca­tion by an enzy­mat­ic colour reac­tion.

In con­trast to this, there is also the pos­si­bil­i­ty of a com­pet­i­tive test set­up. Instead of anti­bod­ies also anti­gens can be used to detect anti­bod­ies in the sam­ple. For this detec­tion are used, among oth­ers, enzy­mat­ic-col­ori­met­ric label­ing with lumi­nes­cence, latex or gold par­ti­cles.

In gen­er­al prac­tice of auto­mat­ed sys­tems the man­u­al steps of a typ­i­cal ELISA are tak­en over by an auto­mat­ed pipet­ting sys­tem so that the analy­sis is per­formed auto­mat­i­cal­ly. These auto­mat­ed sys­tems are main­ly used in med­ical diag­nos­tic rou­tine lab­o­ra­to­ries to process a high­er num­ber of patient sam­ples.

For diag­nos­tic para­me­ters, where the time between sam­ple col­lec­tion and result is cru­cial for the patient, rapid tests are used (Point of Care (PoC) tests), e.g. in form of lat­er­al or ver­ti­cal flow sys­tems. Immunoas­say rapid tests have a sim­i­lar struc­ture to ELISA but typ­i­cal­ly use col­loidal gold for label­ing to allow visu­al eval­u­a­tion.

The com­plete Prod­uct Cycle of an IVD

The devel­op­ment of an IVD starts with the project idea and assess­ment includ­ing the require­ments pro­file fol­lowed by the fea­si­bil­i­ty study. In this study it is exam­ined whether the require­ments can be gen­er­al­ly ful­filled, for exam­ple, whether the mea­sur­ing range can be achieved with the select­ed raw mate­ri­als and test sys­tem. Sub­se­quent­ly, the now rough­ly defined basic con­di­tions are fine-tuned in the actu­al prod­uct devel­op­ment and opti­miza­tion phase.

In trans­fer-to-pro­duc­tion, the man­u­fac­tur­ing process is scaled up. Fur­ther­more, the repeata­bil­i­ty is ver­i­fied so that the final prod­uct is ready for series pro­duc­tion and the process is reg­u­lat­ed, con­trolled, and auditable.

In the final per­for­mance eval­u­a­tion test con­for­mi­ty with the ini­tial­ly defined require­ments is assessed, e.g. in terms of pre­ci­sion, homo­gene­ity, sen­si­tiv­i­ty, recov­ery, and clin­i­cal per­for­mance. These data includ­ed in the tech­ni­cal doc­u­men­ta­tion, which is the basic require­ment for approval to obtain the CE label and launch an IVD on the mar­ket. In order to eval­u­ate the qual­i­ty of the prod­uct, after mar­ket place­ment, post-mar­ket sur­veil­lance is fol­low­ing after­wards. The find­ings may result in adjust­ments of the prod­uct so that the prod­uct cycle starts all over again.

Human & Vet­eri­nary Diag­nos­tics

The prin­ci­ple of a pre­cise and ear­ly diag­no­sis, as the best pre­req­ui­site for a suc­cess­ful ther­a­py, exists for a long time and has not lost its rel­e­vance in view of demo­graph­ic change, the increas­ing num­ber of chron­ic dis­eases, and can­cer diag­noses.

Thy­roid dis­eases like Hashimo­to and Graves’ dis­ease are autoim­mune dis­eases in which the body pro­duces anti­bod­ies against the body’s own pro­teins. These detect­ed autoan­ti­bod­ies can be used for diag­no­sis.

Anoth­er autoim­mune dis­ease is rheuma­toid arthri­tis. For the diag­no­sis well-known bio­mark­ers are used such as rheuma­toid fac­tors and anti­bod­ies against cyclic cit­rul­li­nat­ed pep­tides. Since there is no cure for this chron­ic dis­ease, sci­en­tists are still search­ing for new bio­mark­ers that allow ear­ly diag­no­sis.

Many research approach­es in the field of immuno-oncol­o­gy are also con­cerned with the find­ing of new pos­si­bil­i­ties for diag­no­sis and prog­no­sis as well as ther­a­py mon­i­tor­ing of the dis­ease.

In autoim­mu­ni­ty the focus is on the mea­sure­ment of autoan­ti­bod­ies, where­as in oth­er dis­eases small mol­e­cules are detect­ed. In case of degen­er­a­tive dis­eases, for exam­ple osteoarthri­tis, the degrad­ed frag­ments can be used for diag­nos­tics. In some cas­es, the most sen­si­tive bio­mark­ers are not obvi­ous­ly relat­ed to the dis­ease, a well-known exam­ple is pro­cal­ci­tonin in sep­sis.

Nov­el food, nutraceu­ti­cals, func­tion­al food, etc. are more and more impor­tant in the health sec­tor in addi­tion to clas­si­cal diag­nos­tics and ther­a­py for known and new dis­eases. These foods include pri­mar­i­ly health-pro­mot­ing prop­er­ties such as chia seeds, noni juice, and ste­via.

We devel­oped tests and con­trols for sev­er­al of the list­ed top­ics above and we are in active coop­er­a­tion with sci­ence and indus­try to con­tribute to high-qual­i­ty diag­nos­tic. For iden­ti­fi­ca­tion of new bio­mark­ers we also work with engine the bio­mark­er com­pa­ny. Com­bined with their tech­nol­o­gy over 100.000 poten­tial anti­gens are ana­lyz­able in one step.

In the vet­eri­nary sec­tor the same prin­ci­ples apply as in human diag­nos­tics & med­i­cine, and there­fore we are expand­ing our prod­uct port­fo­lio to biospec­i­mens of ani­mal ori­gin and col­lab­o­rate with part­ners from the Diag­nos­tikNet BB on projects for bio­mark­er-based osteoarthro­sis diag­nos­tics in dogs & hors­es as well as on the devel­op­ment of vet­eri­nary con­trols.

ES SIND INSGESAMT 3 INNOVATIONSASSISTENTINNEN ÜBER DEN EUROPÄISCHEN SOZIALFOND FÜR DEN AUFBAU FOLGENDEN INNOVATIONEN BESCHÄFTIGT:

  1. Den Bestand und die Produktetikettierung durch die Etablierung eines zweidimensionalen Code-Systems modernisieren, wodurch die Lagerflächen effizienter genutzt werden sollen und die Integration des Lagerbestands in eine ERP-Software ermöglicht wird.
    Damit sind folgende Tätigkeiten/Arbeitspakete verbunden:
  • Reevaluieren der aktuellen Lagerkapazitäten
  • Funktionen der Etiketten-Software sichten
  • Geeignete Etiketten-Vorlagen auf Sachdienlichkeit überprüfen
  • Übersetzung von ein- in zweidimensionalen Code
  • Etablierung der Etikettierung in reorganisierte Lagerflächen
  • Prozess zur Etikettierung unterschiedlicher Materialien, einschließlich von IVD, entsprechend der ISO 9001 und Iso 13485, erstellen
  • Schnittstelle zur ERP-Software herstellen
  • Integration des Lagerbestands in ein Lagermodul der Software
  • Durchführungszeiträume: 01.01.2025 – 31.12.2025
  1. Etablierung einer neuen Methode zur Bestimmung der Restfeuchtigkeit von gefriergetrockneten Produkten, um die Präzision der Ergebnisse zu optimieren und die Bestimmung bei Produkten zu ermöglichen, deren Matrix bislang ein Ausschlusskriterium darstellten.
    Damit sind folgende Tätigkeiten/Arbeitspakete verbunden:
  • Literaturrecherche zu Feuchtigkeitsmessungen
  • Inbetriebnahme des Karl-Fischer-Titrators V30S
  • Messreihen mit unterschiedlichen Matrizes durchführen
  • Vergleich der beiden Messsysteme
  • Reevaluieren der intern festgelegten Vorgaben
  • Kurzanleitung zur Bedienung verfassen
  • Freigabedokumente für interne Kalibrierung erstellen
  • Durchführungszeiträume: 01.12.2024 – 30.11.2025
  1. Entwicklung einer Kontroll- bzw. Ringversuchsprobe, die zur Früherkennung von akuten und chronischen Darmerkrankungen genutzt werden kann, und somit die Erweiterung der Angebotsvielfalt des Unternehmens.
    Damit sind folgende Tätigkeiten/Arbeitspakte verbunden:
  • Literaturrecherche zur Stabilisierung von Hämoglobin
  • Artifizielle Stuhlmatrix herstellen
  • Geeignete Aufreinigungsmethode zur Isolierung von Hämoglobin etablieren
  • Hämoglobin durch adäquate Pufferung stabilisieren
  • Funktion von Proteasehemmern auf Hämoglobin überprüfen
  • Hämoglobin in artifizieller Stuhlmatrix untersuchen
  • Unterschiedliche Stabilitätsuntersuchungen mit statistischer Auswertung
  • Überprüfung von Kontraindikationen bei Spendern
  • Überführung des Versuchsaufbaus auf humane Stuhlmatrix
  • Scale-up in den Produktionsmaßstab
  • Durchführungszeiträume: 01.12.2024 – 30.11.2025
Qualification measures:

Growing Organisation; Adaption of Qualification to new market demands, project areas and fields of production

To achieve the goal, that invent persist at the international market, qualification for current and new employees were conducted as follows:

  • training in online-marketing,
  • in contract law and
  • in business basics for executive leadership with scientific background.

New employees acquired competences in the fields of:

  • data protection,
  • medical devices advice,
  • internal auditing,
  • performance assessment of in-vitro diagnostics as well as
  • project management

In the field of production, knowledge of macro programming was gained for digitization.

The measures were funded through the European Social Fund and the state of Brandenburg for the period 2019 – 2021.