The TCB offers a diverse range of training programs within the Healthcare domain, catering to professionals in various capacities and industries. Some of the programs are:

Application of Risk Management to Medical Devices as per ISO 14971:2019 The process described in this standard assists the manufacturer of medical devices in identifying the hazards associated with the medical device, estimating and evaluating the associated risks, to control these risks, and to monitor the effectiveness of the controls. Our training program on ISO 14971:2019 covers the standard in detail and compliance with regulatory requirements. This also includes a systematic approach to risk mitigation throughout the entire product lifecycle. The training equips professionals with the necessary tools to manage risks effectively, comply with regulations, and contribute to the safety of medical devices.To enhance the interactivity and engagement of training programs, real-life scenarios have been incorporated.

Internal Auditor Program as per ISO 13485:2016- This ISO standard specifies the requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. Our training on ISO 13485:2016 covers all the aspects of the standard and compliance with regulatory requirements, it also includes a risk-based approach for developing the management system for medical devices. This training helps learners gain a comprehensive understanding of the standard’s requirements, including quality management principles, risk management, and regulatory compliance.

Medical Laboratory System and Internal Audit as per ISO 15189:2022 – This international standard specifically applies to medical laboratories and contains requirements for the medical laboratory to plan and implement actions to address risks and opportunities for improvement. Our training on ISO 15189:2022 covers the interpretation of all the clauses of the standard and outlines the requirements for quality and competence in laboratory environments.  It also includes the risk-based approach and internal audit. The training program helps the participants to understand the various testing requirements. Benefits of the training include: increasing the effectiveness of the management system, decreasing the probability of invalid results, and reducing potential harm to patients, laboratory personnel, and the environment. To make the training interactive and engaging, exercises with nearly real-life scenarios in the laboratories have been introduced.

ICMED Scheme- Tools for Ushering Quality in Medical Device Industry- The use of medical devices in the field of healthcare has become an integral part in many a treatment carried out by healthcare experts today. As such, these devices can bring the gift of life and normalcy to the patients, but in the case of any error, it can have fatal consequences as well. The need of the hour, then, is to ensure that a standard of quality is maintained throughout the production of such medical devices, and to ensure that overall citizen safety and patient satisfaction is achieved. Through the Training and Capacity Building Cell scheme on ICMED and ICMED plus certification, developed in conjunction with the medical devices industry, the process and production of quality medical devices shall be ensured to create healthy and happy citizens the world over. Inn this training participants will gain the knowledge about Medical Devices- Integral to Healthcare Delivery, about the Quality of Medical Devices. This training module also includes learning about Growing Market of Medical Devices, ICMED Scheme as a Solution etc.