The AI platform for clinical trial report submission

Ensure your submissions are Compliant, convenient and 10x faster

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What is AInonymize?

The AI solution to transform clinical report submission is finally here. Our powerful technology is specifically designed to simplify and streamline the clinical trial report submission process, ensuring compliance with complex data privacy regulations.


Our state-of-the-art algorithms and techniques ensure that your data is fully anonymized and compliant with all regulations including EMA and HC, giving you peace of mind that your data is protected. 


A seamless user-friendly interface makes the submission process a breeze. 


Our platform allows you to collaborate with other stakeholders in real-time, streamlining the anonymization process and saving valuable time.  

Submit CSR documents 86% faster with our AI-driven anonymization solution while ensuring best-in-class risk protection

How AInonymize Works?

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Pharmaceutical companies often face conflicting demands from government agencies enacting data privacy regulations & researchers who require data transparency. Health authorities like EMA, Health Canada, etc., have put into place regulatory requirements for disclosing data for submissions that have to balance between transparency & privacy.

Connect with us to explore our UI/UX-led approach using customized algorithms that take the pain out of complex regulatory compliance.

Manual redaction & anonymization in the pharmaceutical industry is expensive, laborious & error-prone. AI-nonymize brings together

  • Cutting edge AI
  • User-centered Design, and
  • Expert Regulatory Compliance Algorithms

to simplify compliance with the evolving stringent global regulatory disclosure & submission rules.

Here is why you need it!

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Features & Benefits

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