Bioqix Learning Academy - Empowering professionals.
When staff understand ISO requirements and can apply the principles in daily work, organisations see fewer nonconformities, stronger internal audits and faster closing of gaps. Bioqix training workshops are conducted by the most qualified and experienced facillitators The workshops are designed to deliver practical competence, we help you reduce risk, save money and time by providing tailor made sessions at a reasonable price. Join a virtual from anywhere in world, or book an in company training.
ISO 13485:2016 - Internal Auditor
A practical 2-day workshop on the requirements of ISO 13485 and how to plan, conduct and report internal audits. Participants leave able to gather evidence, write findings and manage and support a internal audit programme.
Duration: 1-2 days (virtual)
Format: Live online facilitation
Upcoming dates: 19 - 20 October 2026
ISO 13485:2016 Awareness and Implementation Workshop
A focused session for teams who need a clear working understanding of the standard, their role in the QMS, and what 'audit-ready' looks like day to day.
Duration: 0.5 - 1 day (virtual)
Format: Live online facilitation
Upcoming dates: 09 October 2026
Custom Training Offerings
Need something that is not on the standard list? We can design a virtual workshop around your team, product type and regulatory pathway.
Available on request:
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Fundamentals of Medical Device Regulatory Affairs
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Regulatory writing and technical documentation
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Clinical evaluation
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ISO 14155 (GCP for device investigations)
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Post-market surveillance and PMCF
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EU MDR overview
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IEC 62366 usability engineering
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Clinical quality assurance
ISO 14155 GCP Awareness
A focused session on Good Clinical Practice for medical-device investigations. Covers ISO 14155 principles, roles, informed consent, safety reporting, and essential documents. Suitable for site teams, CRAs, study coordinators, QA professionals or recent graduates.
Duration: 1 day (virtual)
Format: Live online facilitation
Upcoming dates: 07 November 2026