Compliance Certification Programs

You operate in a regulated sector where competence and documentation decide market access. Vicki Partridge offers compliance certification programs that aim to develop practical skills in Australian medical device regulation, with certificates issued upon completion. The programs are designed and delivered by an industry professional with over 30 years of experience and 15 years of experience within the Therapeutic Goods Administration.
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With our programs, you gain training that converts regulatory rules into repeatable processes for your team. The goal is to achieve clear outcomes in submissions, post-market duties, and quality documentation for devices supplied in Australia and other supported jurisdictions. Vicki’s training and certification work spans Australia and the United States, helping you align internal practices with current expectations.

You show credible evidence of staff competence, reduce documentation errors that trigger noncompliance, and standardise knowledge across regulatory, quality, and technical roles. These outcomes reflect the focus of Vicki’s workshops and her extensive experience working with the TGA.

• TGA Essential Principles with practical application
• Post-market surveillance and vigilance obligations
• Quality management systems aligned to ISO 13485
• Audit readiness and effective communication with regulators

​These topics reflect the published workshop themes delivered by Vicki Partridge Pty Ltd.