Safely Accelerate Clinical Document Submissions. Protect Business Interests.
With IQVIA’s Privacy Analytics, you get a flexible, holistic solution to meet your unique transparency needs:
- Meet deadlines for initiatives such as EU CTR, Health Canada PRCI, and EMA Policy 0070.
- Stay true to regulations while protecting participant privacy and identifying and protecting commercially confidential information (CCI).
100%
of sponsors who tried Privacy Analytics over the past three years used our solution for their next dossier
100+
We have supported 100+ successful regulatory submissions since 2017, with many more pending publication
10x
Redacted/anonymized dossiers prepared by Privacy Analytics get 10x fewer transparency warnings published by regulators than the industry average.
You need to accelerate submissions for the broader range of clinical document types you must address throughout the clinical trial life cycle. We give you options.
Redaction-as-a-Service
We reduce the costs associated with redacting clinical study dossiers by 15%-20% or more by uniting our 4th-generation natural language processing tech with automated redaction.
Anonymization-as-a-Service
A unique, utility-preserving approach — peer-reviewed in 200+ publications — performed by world-class experts.
CCI Protection Service
Privacy Analytics is the only company to offer holistic CCI protection—from identification to redaction.
Software License
Deploy our Privacy Analytics Platform on-premise to achieve natural language processing-enabled protection of personal and commercial information.
Want to see case studies and talk to an expert about a complete solution for your document submissions? Let’s talk.
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