9080176326 info@cdaqi.com

What We Do?

Training is teaching, or developing in oneself or others, any skills and knowledge that relate to specific useful competencies.

Training has specific goals of improving one’s capability, capacity, productivity and performance.

In Meditix we are focusing on conducting Regulatory, QMS and Clinical Trainings as per the Client’s requirement.

Medical device coursework is developed and administered by industry-active instructors—satisfying specific disciplines and enhancing cross-discipline exposure.

Medical device training program attendees benefit from lively discussions with peers in an open, interactive setting. The discussion of real-world experiences amongst the instructor and participants allows for expanded viewpoints that can benefit employees daily.

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The different Trainings we can deliver in CDAQi Solutions are listed below:

ISO 13485 Training
  • ISO 13485: International Quality Management Standard for Medical Devices
  • ISO 13485 is an international management standard developed specifically for medical device manufacturers. It provides a harmonized model for creating and maintaining an effective quality management system (QMS) for the design and manufacture of medical devices. This training provides you with an overview of the purpose and requirements of ISO 13485 and how to improve customer relationships, operations and corporate culture by the effective use of a QMS.
  • The training is an introduction for anyone involved in the development, implementation and management of a QMS based on ISO 13485. Upon completing the training, you will be able to interpret all clauses of ISO 13485:2016 and recognize the role of management in implementing and maintaining ISO 13485.
  • The course comprises lecture and workshop exercises.
  • Contact Meditix today to learn more about ISO 13485 Awareness Training.
ISO 14971 Training
  • Applied ISO14971 Medical Device Risk Management
  • The internationally accepted standard guideline for medical device risk management is the ISO 14971 standard.
  • Cdaqi’s training is designed to provide a concise but complete knowledge of medical device risk management to supplement readings of the 80-page standard and to initiate those who are new to the medical device industry.
  • Our focus has been given to explaining the use of key tools such as the Failure Mode and Effects Analysis (FMEA) and the Fault-Tree Analysis (FTA) to enable immediate application in ISO 14971 projects.
  • This training offers a systematic methodology to comprehend medical device risk management and connects the vital elements of risk management methodologies for a more efficient application of principles.
  • This training also provides guidelines on how to conduct productive meetings to construct medical device risk profiles.