Leverage cutting-edge technology to provide timely regulatory updates, predictive analytics and automated workflows. Stay ahead of regulatory changes and ensure continuous compliance for sustained success.
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Medical Devices
and MedTech
Biotech
Pharma (Rx) / OTC
Consumer
Health
CRO
Keeping up with frequent regulatory changes, such as FDA updates or EU directives, can lead to compliance gaps and inefficiencies in drug development and clinical trials.
RegAlerts enables you to stay ahead with timely, accurate, and actionable alerts. Receive instant notifications and in-depth analysis to manage drug development, clinical trials, and regulatory submissions proactively.
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Limited access to comprehensive and actionable compliance insights makes data-driven decision-making challenging, impacting R&D, and maintaining regulatory compliance.
RegInsights unlocks augmented analytics that drive data-informed decisions for R&D and compliance. Optimized workflows and insights ensure regulatory adherence and research success.
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Navigating complex regulatory environments can be difficult due to a lack of reliable and accurate information, increasing risks in drug approvals and market access.
Ask RegASK delivers precise and reliable answers to regulatory queries. Leverage over 1700+ regulatory experts, in over 157 markets to navigate complex environments with ease.
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Integrating multiple compliance tools and processes into a cohesive system is challenging, often leading to inefficiencies and fragmented workflows.
RegGenius integrates multiple AI-Driven capabilities; a GenAI conversational platform, augmented analytics, content summarization and translations. Ensuring efficient management of regulatory submissions, quality compliance, and supply chain operations.
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At RegASK we combine advanced machine learning algorithms with expertise of our regulatory professionals to deliver accurate actionable timely insights.
Leverage RegASK to identify and mitigate regulatory risks with advanced technologies, reducing errors and ensuring accuracy.
RegASK tailors regulatory insights to your specific needs, ensuring relevant and actionable information. Our platform adapts to businesses of all sizes, offering a comprehensive and dynamic approach to compliance management.
RegASK's cutting-edge platform features a powerful task management system that transforms regulatory workflows, empowering you to seamlessly manage every aspect of the regulatory process.
Stay ahead of compliance requirements with RegASK’s timely monitoring, enabling proactive identification of non-compliance issues and generating timely reports.
Todd Chermak R.Ph., Ph.D.
GSVP and Global Business Head Immunology and Proteomics
CellCarta
Regulatory News Australia Medical Devices
On February 5, 2026, the Therapeutic Goods Administration (TGA) published updated guidance clarifying how artificial...
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Europe & Central Asia Regulatory News Medical Devices
On 5 January 2026, the European Commission announced the production release of EUDAMED version 2.22.0,...
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Saudi Arabia Cosmetic and Personal Care Regulatory News Food and Nutrition Home and Industrial Care Medical Devices
On 28 January 2026, the Saudi Food and Drug Authority announced an advisory highlighting its...
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Regulatory News United Kingdom Pharma and Biotech
On 9 February 2026, the UK Medicines and Healthcare products Regulatory Agency (MHRA) published new...
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Regulatory News Medical Devices Finland
On January 19, 2026, Finnish Medicines Agency (FIMEA) published guidance on the use of artificial...
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Regulatory News Food and Nutrition Medical Devices Pharma and Biotech
On January 21, 2026, the U.S. Food and Drug Administration (FDA) announced the launch and...
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