Artixio, a leading provider of regulatory compliance training, today announced the launch of its Medical Devices Regulatory Training program for students and working professionals. The program is designed to provide participants with the knowledge and skills they need to comply with the latest medical device regulations.
The Medical Devices Regulatory Training program covers a wide range of topics, including:
The Medical Device Regulation (MDR)
The In Vitro Diagnostic Medical Device Regulation (IVDR)
ISO 13485:2016
Risk management
Clinical evaluation
Post-market surveillance
UDI
Notified bodies
The program is delivered by experienced regulatory experts who will help participants understand the regulations and how to apply them to their specific products. Participants will also have the opportunity to network with other medical device professionals and learn from their experiences.
“The medical device industry is constantly evolving, and it is important for professionals in this field to stay up-to-date on the latest regulations,” Yog Raj, CEO of Artixio. “Our Medical Devices Regulatory Training program is designed to provide participants with the knowledge and skills they need to comply with the latest regulations and ensure the safety and effectiveness of their products.”
The Medical Devices Regulatory Training program is available in a variety of formats, including:
In-person classroom training
Virtual online training
Self-paced e-learning
The length of the program varies depending on the format you choose. In-person classroom training typically lasts for 2-5 days, while virtual online training and self-paced e-learning can be completed in as little as 1-2 weeks.
About Artixio:
Artixio is a leading provider of regulatory compliance consulting, staffing services and training for the life sciences industry. The company offers a wide range of training programs, including courses on medical devices, pharmaceuticals, and clinical trials. Artixio’s training programs are delivered by experienced regulatory experts who help participants understand the complex regulatory requirements and apply them to their specific products.
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