Conduct training for your management and employees on Introduction to ISO 13485 quality management systems and medical device industry regulatory requirements. Also training on individual SOP’s as required, i.e. risk management, CAPA, complaint handling, management review, root cause analysis, design controls, process validation etc.
We can provide internal auditor coaching during any internal audits we conduct of your QMS, or we can provide through our consulting partners, Certified Internal Auditor training. If you use our SOP for Internal Auditing this would include training for this procedure.
We can set you up with Accredited Certification Lead Auditor Training through our consulting partners. We can further support your lead auditor training during any internal audits we assist with during your ISO 13485 quality management system implementation.
Meet all the regulatory requirements in advance
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