Instructor

Joanna Jackson

With more than 20 years in medical device Quality and Regulatory, including 10 years in Regulatory Affairs, Joanna Jackson has extensive hands‑on experience guiding companies through compliance challenges and global regulatory pathways without losing sight of the business perspective. She is passionate about making regulatory requirements practical and accessible as well as providing coaching to newly appointed PRRCs and leadership teams working with market expansion.

Joanna is known for her analytical approach, combined with a positive attitude and strong communication skills. She is consistently appreciated for her supportive and collaborative style.

Related courses to Joanna Jackson

Becoming a Regulatory Affairs Manager for Medical Devices – Course

Get the knowledge and skills needed to lead the RA function at a medical device organization. Interpret and apply MDR, IVDR, and ISO 13485 effectively.
Oct 6
- Oct 7, 2026
Copenhagen, Denmark
Post market, Quality management and QA, Regulatory Affairs

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