Future proof your compliance strategy

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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Your Regulatory Solution

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Challenge

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.

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Solution

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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Challenge

Limited access to comprehensive and actionable compliance insights makes data-driven decision-making challenging, impacting R&D, and maintaining regulatory compliance.

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Solution

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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Challenge

Navigating complex regulatory environments can be difficult due to a lack of reliable and accurate information, increasing risks in drug approvals and market access.

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Solution

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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Challenge

Integrating multiple compliance tools and processes into a cohesive system is challenging, often leading to inefficiencies and fragmented workflows.

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Solution

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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Why RegASK

Why Regask

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.

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“RegASK provides us with customized, timely and actionable regulatory intelligence to ensure compliance with the dynamic global regulatory environment, and drive a competitive advantage for our business. We are pleased with our decision to partner with RegASK.”

Todd Chermak R.Ph., Ph.D.
GSVP and Global Business Head Immunology and Proteomics
CellCarta

Resources

EU Announces Landmark Reform of Pharmaceutical Legislat…
On 11 December 2025, the European Commission announced a political agreement on a major reform of EU pharmaceutical legislation, marking the…
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US FDA Announces Deployment of Agentic AI Capabilities …
On December 1, 2025, the U.S. Food and Drug Administration (FDA) announced the deployment of new agentic AI capabilities to enhance pre-mark…
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EU Council Approves Postponement of Chemical Packaging …
On 17 November 2025, the Council of the European Union approved a regulation postponing several upcoming compliance deadlines under the revi…
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HSA Singapore Issues Updated Guidance on Medical Device…
On 5 November 2025, the Health Sciences Authority (HSA) of Singapore released new guidance documents outlining regulatory requirements for m…
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Global Regulators Confirm No Link Between Paracetamol U…
Between September 23–26, 2025, multiple health authorities, including Singapore’s Health Sciences Authority (HSA), Australia’s Therape…
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U.S. Launches Investigation into Medical Device and PPE…
On September 26, 2025, the U.S. Department of Commerce’s Bureau of Industry and Security (BIS) announced a Section 232 investigation into …
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