Advice on certification processes for manufacturers and laboratories

Advice on certification processes for manufacturers and laboratories.

Created to study and advice on developing a quality management system for new test laboratories and medical device developers that fit the best to ensure that all medical device processes are taken into account.

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Designed to bring your company through the certification process by ISO IEC 17025 regulation and ISO 13485 international standards focused on the design and production of safe and effective medical devices based on technology and scientific research.

 

Leaders

  • Ing. MSc. Javier Hernando García Ramos. 
  • Ing. MBA Juan Guillermo Barreneche Ospina.

 

Associated Researchers

  • Ing. MSc (c) Juan Camilo Guerrero Valencia.
  • Ing. Mónica Yaneth Ruiz López