Evaluating the presence of software-as-a-medical-device in the Australian Therapeutic Goods Register by Ceross, A, Bergmann, J

Tracking the presence of software as a medical device in US Food and Drug Administration databases: Retrospective data analysis by Ceross, A, Bergmann, J

Topic modelling for risk identification in Data Protection Act Judgements by Ceross, A, Simpson, AC

The use of data protection regulatory actions as a data source for privacy economics by Ceross, A, Simpson, A

Assessment of medical device regulator COVID-19 policies on entry to market for prioritised devices: a case study by Bergmann, J, Ceross, A

Rethinking the proposition of privacy engineering by Ceross, A, Simpson, AC

The efficacy potential of cyber security advice as presented in news articles by Quinlan, M, Ceross, A, Simpson, A

More than red tape: exploring complexity in medical device regulatory affairs by Han, Y, Ceross, A, Bergmann, J

Using rule-based decision trees to digitize legislation by Mingay, HRF, Hendricusdottir, R, Ceross, A, Bergmann, J

Evaluation of large language models for the classification of medical device software by Han, Y, Ceross, A, Bourgeois, F, Savaget, P, Bergmann, JHM