The company shall implement a high standard of performance for the products to ensure each batch is produced at consistently high quality and meets the relevant international regulatory requirements.
The company shall strive to supply the customers with quality products and services that will meet or exceed their expectations and match the knows state of the art.
The company shall provide a conducive workplace, suitable trainings and a growing career development to increase the employee’s commitment, qualification and satisfaction.
VeroTest has a Quality Management System that is successfully certified as per ISO13485:2016 standard. The company is also registered with the Medical Devices comptent authority in Malaysia name Medical Device Authority (MDA).
Our products that are non Annex II (list A and B) as per the IVD directive 98/79/EC are CE Marked for professional use.
We are committed to adhere to regulations and requirements needed in any country where our products are marketed.
ISO 13485:2016
MDA Establishment License
VeroTest CE Declaration - Febrile Antigen
VeroTest CE Declaration - Latex Agglutination Kits
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