Quality

Regulation

Compliance

Dr. Korman Laboratories Ltd.’s activities are conducted under a certified quality system according to ISO 9001:2008, ISO13485:2003 and EN/ISO 13485:2012.
Dr. Korman Laboratories Ltd.’s production premises are designed, built, maintained and qualified through periodic environmental monitoring and validations of the clean rooms, in thus complying with the EU cGMP requirements for Class 5 clean rooms.
All production and distribution records allow backward and forward traceability of the products.
Dr. Korman Laboratories Ltd.’s products are medical devices classified as Class III according to 93/42/EEC Directive.
The hyaluronic acid products indicated for bio-revitalization and intra-­articular application are pending CE approval.

We Offer

A range of 8 (eight) different RADIANT cross-linked HA dermal fillers
Will provide you the versatility needed to correct the facial contours from the deepest volumes till the most superficial wrinkles and restore the radiance of the skin.
A range of 5 (five) bio-revitalization products
Manufactured from hyaluronic acid and hyaluronic acid + glycerol.

Raw Material

A state of the art European manufacturer of Pharmaceutical/Medical Grade.
(European Monograph N ° 1472) provides the raw material of the Hyaluronic Acid products; this guarantees the highest quality of Hyaluronic Acid products.
The Sodium Hyaluronate is provided with a molecular weight of 3000 kD.