At ToskaniMED, safety and clinical precision define each of our products.

All our injectables are developed and manufactured in strict compliance with the applicable European regulations for medical devices, guaranteeing the highest standards of quality, safety, and clinical performance.

Before being marketed, each product undergoes a thorough evaluation that includes:

• Verification of biocompatibility, according to ISO 10993 standards
• Safety and performance assessment based on scientific and clinical evidence
• Stability and sterility studies that ensure integrity throughout the product’s shelf life
• Validation of critical processes, including sterilization and packaging systems

All products carry the corresponding CE marking after passing conformity assessment procedures under the supervision of notified bodies.

Manufacturing is carried out under strict quality standards according to ISO 13485, ensuring full control at every stage of the process, from design to distribution. This guarantees complete traceability, batch consistency, and ongoing compliance with regulatory requirements.

Before release to the market, each batch undergoes rigorous physical-chemical, microbiological, and functional quality controls.

Additionally, ToskaniMED maintains a robust post-market surveillance (PMS) and clinical follow-up system, ensuring continuous monitoring of the performance and safety of its products under real use conditions.

Because in aesthetic medicine, trust is built with science, control, and an absolute commitment to patient safety.