BioFilm operates a rigorous Quality Management System at all levels of the business. The quality and safety of our products is paramount and relies on the competence of our employees and procedures.
We are, therefore, committed to adhering to the latest international standards through involving staff in all aspects of quality and food safety and requiring them to participate in regular training programmes.
Our Quality Management System meets the requirements of ISO 13485:2003, the quality system regulations of the US FDA and cGMP (current good manufacturing practice).
All of our medical devices products comply with the EU Medical Device Directive 93/42/EEC.