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IVD

We are an EN ISO 13485 certified EU-located company developing and producing CE IVD real-time PCR kits.

Our in vitro diagnostics fall into five categories: clinical genetics, hematology, pharmacogenetics, oncology and microbiology.

Our typical partners are end-users of the RT-PCR kits (mostly in CZ and SK), business partners and distributors. We are looking for business partners and/or distributors worldwide who can fit the portfolio of our products, either the whole or a part of it, to their sales strategy (see here).

gb SARS-CoV-2 Variant E484K, L452R gb SARS-CoV-2 Variant E484K, L452R

gb SARS-CoV-2 Variant E484K, L452R gb SARS-CoV-2 Variant E484K, L452R

Multiplex CE IVD kit enables detection of SARS-CoV-2 virus RNA and simultaneously the detection of mutations E484K and L452R in one reaction. The kit is based on one-step RT-qPCR using fluorescently labelled probes (FAM, HEX, ROX channels) and exogenous positive control (Cy5 channel).

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gb PHARM DPYD gb PHARM DPYD

gb PHARM DPYD gb PHARM DPYD

The CE IVD kit is used for determination of genotype of four polymorphisms according to guidelines CPIC and DPWG: *2A (c1905+1G>A), *13 (c1679T>G), HapB3 (c1236G>A) and c2846A>T in human genomic DNA. The principle of detection is based on real-time PCR with fluorescently labelled probes (allelic discrimination).

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