Laboratory
The IMC laboratory, certified ISO 9001 and ISO 13485, as well as bearing the CE marking, is committed to ensuring the quality of its products by adhering to international standards and regulations. To this end, we conduct a series of rigorous tests on raw materials, finished products, and those in production.
We perform strict physical, chemical, and microbiological controls, in accordance with international references and standards, with approximately 200,000 tests conducted each year, including pharmacopoeias and ISO standards. IMC ensures the compliance of its products before they are marketed.
Our Certificates
ISO 9001
The ISO 9001 certification attests to our commitment to a rigorous quality management system. It guarantees that our processes are standardized, efficient, and focused on customer satisfaction.
ISO 13485
The ISO 13485 standard is specific to medical devices. It demonstrates our ability to provide medical products that comply with the strictest regulatory and safety requirements.
CE Marking
The CE marking confirms the conformity of our products to European safety and performance standards. It demonstrates our commitment to adhering to the most demanding market regulations.
Our Laboratories
Quality Control Laboratory for Medical Devices
Quality control laboratory for Medical Devices according to ISO, ASTM, and European Pharmacopoeia standards.
Quality Control of Solutions
Quality control laboratory for bulk solutions, injectable products, and concentrated solutions for Hemodialysis (Ph Eur, ISO).
Official Accreditation
Laboratory accredited by the National Agency for Pharmaceutical Products, ensuring the highest standards of quality and safety.