ISO 13485 Certificate This standard determines the terms of the quality management system which can be used by organizations involved in the design, production, installation and servicing of medical devices and related services. More Training ISO 13485 Documentation Training ISO 13485 Informational Training ISO 13485 Internal Auditor Training 93/42 EEC Medical Device Director Training Clinical Evaluation Training (Meddev 2.7.1 Rev.04) ISO 14971 Risk Analysis Training More Clinical Evaluation Consulting More CE Certification Consulting More

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TıbbiCe Consulting

Training and Validation Services

TıbbiCE Consulting, Training and Validation Services, offers consulting, training and validation services to domestic and overseas medical device producers during their CE and ISO 13485 Certification (93/42/EEC) process. With its expert staff from different backgrounds including but not limited to biology and biomedical, mechanical and metallurgy engineering, TıbbiCE Consulting, Training and Validation Services is the medical device consulting company with the largest expert staff in Turkey.

TıbbiCE Consulting, Training and Validation Services’ principle for product and quality management system is to give a “Purpose-driven, Solution and Customer Satisfaction Oriented” service that grounds on data confidentiality with its expert consultants.
We share the knowledge and experience we have gained in 9 years through working with more than 140 medical device producers and being involved in the CE and ISO 13485 Certification processes of more than 300 medical devices. We conduct the certification process professionally and aim to complete it in optimum time.


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