Eurogentec offers cGMP custom manufacturing services for oligonucleotides that are part of IVD kits or lab-developed tests. Our cGMP production process and Quality Management System is compliant to ISO13485:2003 and FDA 21 CFR Part 820. EUROGENTEC is registered as an ASR manufacturer with the FDA under registration number 3003830126.



For details about our cGMP custom manufacturing services for diagnostic oligonucleotides, click here to discover our Diagnostic pages.

For inquiries, please contact the Eurogentec Diagnostic Oligonucleotides or Taq  team:

Diagnostic Oligonucleotides	Diagnostic Taq
Europe Tel: +32 (0)4 372 74 00 Fax: + 32 4 372 75 00 diagnostic.oligo@eurogentec.com	Europe Tel: +32 (0)4 372 74 00 Fax: + 32 4 372 75 00 diagnostic.taq@eurogentec.com
North America Tel: +1 858 793 2661 Fax: +1 415 680 1686 diagnostic.oligo.us@eurogentec.com	North America Tel: +1 858 793 2661 Fax: +1 415 680 1686 diagnostic.taq.us@eurogentec.com
Asia Tel: +81(0) 76411 0277 (Japan) info@n-egt.com	Asia Tel: +81(0) 76411 0277 (Japan) diagnostic.taq.jp@eurogentec.com