GMP, ISO 22716, ISO 13485

The evaluation of manufacturing facilities and audits of the producer documentation are services we offer in order to check whether a given medicinal product is manufactured in an appropriate way that guarantees its high quality and patient safety.

The scope of our services includes preparing audits and evaluations of:

  • procedures, documentation of producers of active substances and medicinal products for their compliance with GMP,
  • procedures, documentation of producers of foods
    (dietary supplements/foods for special nutritional uses) - ISO 22000,
  • procedures, documentation of producers of cosmetic products - ISO 22716,
  • procedures, documentation of producers of medical devices - ISO 13485,

We also offer our clients services including preparing documentation and implementing ISO 22716 and ISO 13485 systems and releasing batches of medicinal products for sale (QP).