ro / eng
manufacturing process takes place in a very modern factory equipped with air
pollution, temperature & humidity control devices, sanitized spaces and
All production lines are audited and certi-fied by the National Medicines and Medical Devices Agency in accordance with the Good Manufacturing Practice (GMP) Guideline, a quality standard which provides norms for medicine manufacturing in Europe. The production lines are also certified according to EN ISO 9001.
product series are issued by Qualified Individuals who are certified in
accordance with UE Directives and Good Manufacturing Practices (GMP).
Pharmaceutical forms and annual capacity:
• Liquids (solutions and syrups)
• Solids (tablets and solid forms)
• Soft gelatine capsules