Prevention has never been so simple, practical and affordable to everyone, everywhere

Vision / Mission
History / Numbers

DISCOVER PRIMA Lab SA

OUR VISION

Our vision is to help achieve a world where pathologies can be identified before medical treatment is needed.

We care about everyone’s health: this is why we believe that good and constant prevention is the best means for a healthy and quality lifestyle. Proper prevention is better than a good treatment.

We offer CE-marked IVDs that help people monitor their health frequently and support healthcare professionals in quickly identifying certain diseases.

OUR MISSION

The cornerstones of our work concern the quality of our products, the passion that distinguishes our team and the constant collaboration to achieve the best result possible.

Our tests are made in Switzerland according to the highest quality, from research and development in the laboratory to packaging our kits.

Our best results come from the great passion for our daily work: the production chain is totally in-house, from development to finished product’s distribution

We are convinced that great achievements can only be realized with a good teamwork: relationships, both inside and outside the company, are fundamental into reaching our goals.

OUR HISTORY

ISO 9001 and ISO 13485 certified, we have been investing in quality, research and innovation since 2014.

2014

The company was born from the idea of its passionate founder

2015

The company achieved its first quality certification, ISO 9001

2016

ISO 13485 certification on medical devices was obtained

2017

The Celiac Test is the first IVD made entirely in-house

2018

Expansion of the R&D and packaging departments

2019

Expansion of the offices’ area

2020/21

Construction of the new headquarters, with a production area of about 4.500 m²

CERTIFICATIONS

We worked hard to obtain our first quality certification in 2015, ISO 9001 and, subsequently, ISO 13485 in 2016.

ISO 9001 certification, published for the first time in 1987, defines the necessary requirements for the implementation of a quality management system that regulates business processes.

ISO 13485 certification identifies a specific quality system regulatory standard for companies operating in the medical sector. It includes both aspects of ISO 9001 and specific requirements for the medical device market.

The CE marking, through the affixing of the relative mark, communicates to all interested parties that the product complies with all the requirements established by the EC Directives.

NUMBERS

30 rapid tests

50+ employees

20+ MIO tests sold in 30+ countries