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We have established the quality assurance system which enables us to achieve our prime mission as a company that is to deliver quality, safe and effective products to meet the highest expectations of our patients.
Multi-level quality control involves every stage of the manufacturing processes from a selection and audit of pharmaceutical substances manufacturers, an adequate control for each process step to the finished products quality and products delivery to our customers.
State-of-the-art equipment from the leading manufacturers in Europe and the US for our laboratory complex enable us to test all critical parameters of the starting materials used in manufacturing process and finished products.
Validation laboratory manages the main issue of our compliance with the GMP regulations through validation/qualification of our equipment, premises, analytical methods, cleaning procedures and processes. The independent audit, held in December 2008, verified European standards for validation adopted by our laboratory.
High quality of “Max-Well” products is ensured through:
- highly qualified and experienced personnel;
- pharmaceutical ingredients that meet the leading pharmacopoeias' requirements;
- strict adherence to the quality assurance system requirements;
- multi-level control of the manufacturing process;
- testing of starting materials, semi-product and finished products in certified laboratories; recording of test results;
- critical process operations monitoring on a regular basis;
- qualification/validation of equipment, manufacturing area, analytical methods, cleaning procedures and processes;
- state-of-the-art facility and analytical instruments.
Our Quality Assurance System enables us to guarantee the high quality of our products!
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