The Secret to Faster Clinical Document Submissions?

The Secret to Faster Clinical Document Submissions?

Mirage Software, Powered by Natural Language Processing

As a clinical trial sponsor, you were already facing tight timelines and resource constraints in handling regulatory requirements for document anonymization and redaction.

Now, with the full introduction of the EU Clinical Trials Regulation, you need to handle increased transparency requirements on top of the existing requirements under Health Canada Public Release of Clinical Information and future requirements under EMA Policy 0070.

In this webinar, Niamh McGuinness, Clinical Trial Transparency Expert at Privacy Analytics, showcases Privacy Analytics’ Mirage software. It’s powered by natural language processing and can deliver high-speed redaction or statistical anonymization, helping you meet your regulatory submission deadlines while protecting privacy.

You’ll see a product demonstration and find out which of three solution options best meets your most pressing clinical document submission needs: Redaction-as-a-Service, Anonymization-as-a-Service, or a license option.

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About this webinar

As a clinical trial sponsor, you were already facing tight timelines and resource constraints in handling regulatory requirements for document anonymization and redaction.

Now, with the full introduction of the EU Clinical Trials Regulation, you need to handle increased transparency requirements on top of the existing requirements under Health Canada Public Release of Clinical Information and future requirements under EMA Policy 0070.

In this webinar, Niamh McGuinness, Clinical Trial Transparency Expert at Privacy Analytics, showcases Privacy Analytics’ Mirage software. It’s powered by natural language processing and can deliver high-speed redaction or statistical anonymization, helping you meet your regulatory submission deadlines while protecting privacy.

You’ll see a product demonstration and find out which of three solution options best meets your most pressing clinical document submission needs: Redaction-as-a-Service, Anonymization-as-a-Service, or a license option.

Presenter

Niamh McGuinness is a technical lead with Privacy Analytics’ Clinical Trial Transparency (CTT) business unit. Her team works with a variety of clinical trial sponsors that have turned to us to meet the stringent requirements of regulations such as EMA Policy 0070 and Health Canada Public Release of Clinical Information (PRCI). Drawing on her academic research background, Niamh has helped develop Privacy Analytics’ CTT methodology and our proprietary toolsets.

Niamh McGuinness

Senior Manager of Clinical Trial Transparency and Privacy

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