PT. KalGen DNA was established in 2012, is a joint venture between PT Bifarma Adiluhung (a subsidiary of PT Kalbe Farma Tbk.) and a Malaysian company, DNA Laboratories Sdn. Bhd., which is a leading provider of genetic screening and molecular diagnostic services and products in Malaysia.
Our commitment to quality and improvement are demostrated by well-trained molecular analyst, certification by WHO LabNet proficiency test, ISO 13485, obtained CPAKB, CDAKB permit from Ministry of Health. We will continue to develop innovative diagnostic kits in the area of personalized healthcare to improve human health and well-being.
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To Improve Human Health and Well Being through Innovative Diagnostic Kits.
To be The Most Reliable Partner of High Quality Diagnostic Kits, driven by Innovation and Excellent Management
A well-proven way to prevent cervical cancer is to have screening test. Cervical cancer can affect anyone with a cervix who has ever been sexually active.
KalGen DNA as a marketing for cervical cancer screening test, cooperate with collaborator laboratory, encourage anyone with a cervix who has been sexually active to be screened for cervical cancer.
The fact that cervical cancer rarely presents any symptoms in its early stages highlights the importance of regular screening for the disease.
The main goal of cervical screening is to detect and treat precancer before cancer develops.
HPV XpressMatrix™ is an In Vitro Diagnostic (IVD) test kit, based on the use of target amplification and hybridization methods for the detection of the following 21 HPV genotypes:
High Risk:
HPV 16, 18, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 68
Low Risk:
HPV 6, 11, 42, 43, 44, 81
Elva Diagnostic SARS-CoV-2 Real-time RT-PCR Kit is a real-time RT-PCR in vitro diagnostic test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 virus in human oropharyngeal swab and nasopharyngeal swab specimens .
Elva Diagnostic SARS-CoV-2 Saliva Nucleic Acid Test Kit is a reverse-transcription loop-mediated isothermal amplification (RT-LAMP)-based in vitro diagnostic assay intended for the qualitative colorimetric detection of SARS-CoV-2 virus nucleic acid in the saliva specimen.
AmpFire HPV Screening 16/18/HR is an in vitro diagnostic kit (IVD) for isothermal-based nucleic acid amplification with a real time fluorescence detection method to detect the presence of DNA from the Human papillomavirus (HPV) virus genotypes 16, 18, 31, 33, 35, 39 , 45, 51, 52, 53, 56, 58, 59, 66, 68 qualitative, and specific identification of HPV16 and HPV18 subtypes from various types of samples.
