DiaSys India is a global leader in the design and development of high quality, reliable and innovative clinical diagnostic equipment in clinical chemistry, hematology, urinalysis and point-of-care testing.

DiaSys is following its mantra “Choosing Quality” to be a solution provider for quality products, systems and services! Our focus on understanding customer needs and demands, to create the best possible offering for them, has enabled us to gain acceptance and presence all over India at key institutions but also in rural places.

News & Updates

2020-04-02
"QDx InstaLyte" awarded as the “Most Innovative Product of the Year” at the 10th MT India Healthcare Awards 2020 hosted by Medical Fair 2020 in Mumbai.

QDx InstaLyte- World’s First Truly Modular Electrolyte Analyzer gets awarded as the “Most Innovative Product of the Year” at the 10th MT India Healthcare Awards 2020 hosted by Medical Fair 2020 in Mumbai. It is one of the biggest platform in India where innovative products across IVD industry are screened through multiple rounds and the winner is awarded as “Most Innovative Product”. MT India Healthcare Awards is a completely unbiased platform where results are decided solely on the basis of the merits, the product possesses. The award ceremony took place on 6th March 2020 at NESCO, Mumbai in the presence of Key opinion leaders across In-vitro diagnostics Segment. A proud moment for the entire DiaSys Group as DiaSys India receives this prestigious award for the year 2020.
Read more

2020-04-02
DiaSys India has been awarded the EN ISO13485:2016 QMS certificate for its Mahape, Navi Mumbai facility

DiaSys India has been awarded the EN ISO13485:2016 QMS certificate on 10th February 2020, for its Mahape, Navi Mumbai facility. The audit was extensively carried out by TUV SUD South Asia under the scope of “Manufacturing & Distribution of In-Vitro Diagnostic Products (Biochemistry & Hematology Reagents, Rapid Test Strips) and Analyzers”. DiaSys India will also soon be among the only five IVD companies in India today who have certified for the ICMED 13485, the Indian Certification for Medical Devices (ICMED) -Quality Management systems for regulatory purposes. TUV SUD South Asia was the certification body for this too. The ICMED 13485 certificate scheme was developed by the Government of India, its accredited certification bodies and the Indian Medical Device Industry represented by the Quality Council of India (QCI), the National Accreditation Board for Certification Bodies (NABCB) and Association of Indian Medical Device Industry (AIMED) respectively. This certification is based on the ISO 13485 - Medical devices – Quality management systems and is aimed to encourage Indian companies to manufacture quality medical devices and enhancing credibility and competitiveness. This certification will help our company in reaching out wider in the Indian market, and scale up our operations as it further enhances confidence among buyers.
Read more

Show all news

Exhibitions