+ We monitor the outcomes of our work by defining and applying quality indicators:
+ we carry out internal audits and evaluate their results, which allow not only to control the correctness of the functioning quality system, but also constantly improve it.
+ we implement measures to eliminate repetition of reported defects and check their effectiveness,
+ we thoroughly analyze each and every complaint,
+ We comply with pharmacovigilance standards.
+ We operate in accordance with Good Distribution Practices.
+ We continuously involve all employees in the processes of improving the quality and safety of products.
+ We employ excellent specialists who are highly aware of their actions; we care about the development of their qualifications and working environment.
+ We constantly improve and maintain at the topmost level the Integrated Quality Management System, which includes:
Pharmaceutical quality system
Good Manufacturing Practices (GMP)
is a system based on manufacturing, control and quality assurance procedures that ensure that the manufactured medicinal products meet the specific quality requirements.
Part of the GMP consists of: Quality Control (QC)
concerning sampling, performance of tests on specific product characteristics and properties, comparison of the results obtained with the requirements and specifications
Quality Risk Management (QRM)
quality risk management, i.e. a systematic process of evaluating, controlling, communicating and reviewing the risks to the quality of the medicinal product throughout its life cycle
+ As one of the few companies in Poland, we have the appropriate knowledge, technological facilities and machinery to produce all available forms of medicines, including: tablets, capsules, creams, ointments, gels, syrups, suspensions, powders, sachets in our own factories.