#USA #Princeton #GenAI #Regulatory Writing #ZYLiQ

ZYLiQ Expands Automation in Regulatory Writing with Version 4.0

Introduction
On October 22, 2025, ZYLiQ, a noted leader in AI/ML-driven solutions for regulatory medical writing, announced the launch of its Version 4.0. This new iteration significantly enhances automation and efficiency in Clinical Study Report (CSR) generation and introduces new regulatory document modules. This initiative not only reflects ZYLiQ's commitment to innovation but also aims to improve overall client experiences.

Key Features of Version 4.0
One of the most significant upgrades in ZYLiQ's Version 4.0 is its ability to accelerate CSR creation by an impressive 75%. This remarkable improvement underscores the platform’s capability in meeting the increasing demands of regulatory writing without compromising quality. Major enhancements include:

• - Automatic Source Type Prediction: For sections added by users, the system predicts the appropriate source type, reducing manual input and errors.
• - Optimized Synopsis Creation: This feature allows for faster synthesis and summarization of critical information, ensuring that essential details are incorporated efficiently.
• - Verb Tense Conversion and Text Generation: Leveraging innovative GenAI, the system can intelligently convert tenses and optimize text, providing clearer summaries and conclusions.
• - AI-Assisted Safety and Efficacy Sections: The automated writing for these sections promises accuracy and consistency, vital for regulatory compliance.

Additionally, ZYLiQ 4.0 expands its services with new modules tailored for various regulatory documents that employ GenAI capabilities:

• - Safety Narratives: This feature extracts and assembles data from listings, SDTM/ADaM datasets, and patient profiles, dramatically shortening the time required for completion by up to 90%.
• - Informed Consent Forms (ICF): By integrating content from protocols and investigator brochures, the ICF module aids writers in generating compliant documents more swiftly.
• - Plain Language Summaries (PLS): Automatically creates summaries in everyday language from CSRs, making the data accessible to non-specialists.
• - Protocol Summaries in Plain Language: This module simplifies protocol summaries for better understanding by broader audiences.
• - Confidential Information Masking: ZYLiQ's advanced anonymization feature ensures that sensitive information within all documents remains protected.

Free Pilot Program
To validate the enhancements, ZYLiQ offers potential clients a complimentary two-week pilot program that allows direct comparison between legacy processes and ZYLiQ's automated solutions. This hands-on trial demonstrates the platform's efficiency and effectiveness in real-world applications.

Comment from Management
Farha Feroze, the inventor and product management director at ZYLiQ, expressed her enthusiasm regarding the new release. "Our focus on automating regulatory documents—not merely diversifying types—has led us to develop a remarkably effective solution. With Version 4.0, we are excited to extend our innovation from CSRs to other regulatory documents. I am proud of my team’s efforts to adopt advanced technologies and optimize use cases."

About ZYLiQ
With an experience of over three decades in the CRO landscape provided by Symbiance, ZYLiQ blends extensive life sciences knowledge with proven AI/ML innovations. This dynamic combination allows ZYLiQ to meet diverse client needs across the regulatory writing landscape.

For interested parties, ZYLiQ is currently offering demos and consultations. To learn more, connect with ZYLiQ at zyliq.ai or call +1 949-878-2121.

By adopting such cutting-edge technology in its solutions, ZYLiQ reinforces its position as a key player in the evolving world of regulatory documentation, helping companies navigate the increasingly complex regulatory landscape with greater efficiency and accuracy.

Conclusion
ZYLiQ's Version 4.0 marks a significant leap in the regulatory writing sphere, demonstrating the power of combining AI/ML with industry-specific needs. As companies increasingly seek ways to enhance compliance and documentation efficiency, ZYLiQ's innovations pave the way for a smarter, more streamlined regulatory writing process.