Training

Our Training Modules

 1.   Regulatory Awareness Training

Stay ahead of regulatory changes with our dynamic courses that cover the latest updates and trends in the medical device industry in key jurisdictions such as the EU, UK, USA and Canada.

2.   QMS Overview Training

Master the fundamentals of Quality Management Systems (QMS) to enhance product quality and compliance with international standards.

3.   Audit/Inspection Preparation Training

Prepare your team for regulatory audits and inspections, ensuring a smooth and successful process.

4.   MDR/IVDR Training

Navigate the transition to the new Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) seamlessly with our specialised courses.

5.   MDSAP Training

Understand the requirements of the Medical Device Single Audit Program (MDSAP) to streamline your global regulatory compliance efforts.

6.   Risk Management Training

Learn effective risk management strategies to help ensure the safety and efficacy of your medical devices in accordance with EN ISO 14971.

7.   Customised Training Solutions

Tailor our training programs to meet your specific organisational needs and challenges.

Why Choose MD Compliance?

• Expert Trainers: Learn from industry experts with extensive experience in medical device regulatory affairs.

• Interactive Learning: Engage in hands-on activities and case studies for practical application of regulatory concepts.

• Flexible Training Formats: Choose from in-person workshops or live webinars to fit your schedule.
  

• Compliance Assurance: Equip your team with the knowledge and skills needed to achieve and maintain regulatory compliance.

• Certificates of Completion: Receive personalised certificates upon successfully completing our training programs.