The production process is carried out in a factory equipped with modern production lines, with air, humidity and temperature control devices, with clean rooms and HEPA filters.
All production lines are audited and certified by the National Agency for Medicines and Medical Devices following the Guide to Good Manufacturing Practice (GMP), the quality standard that sets the standards for the manufacture of medicines at European level. At the same time, the production lines are EN ISO 9001 certified.
Also, the product series are issued by Qualified Persons certified according to the EU directives and the Guide on Good Manufacturing Practice for medicinal products for human use.
Pharmaceutical forms and annual capacities:
• Liquids (solutions and syrups)
• Solid shapes (tablets and dragees)
• Soft gelatin capsules