REGASK SPEAKS AT GCC PV TRAINING 2026
Meet RegASK at GCC Pharmacovigilance Training 2026, where pharmacovigilance, drug safety, and regulatory professionals from across the Gulf region come together to explore emerging requirements, practical strategies, and digital innovation in patient safety.
DATES
June 24-25, 2026
VENUE
Mövenpick Grand Al Bustan Dubai, Dubai, United Arab Emirates
THE CHALLENGE
As Pharmacovigilance requirements evolve across the Gulf region, PV teams must align local obligations, global processes, and inspection expectations while maintaining patient safety.
01
Regional expectations continue to change, creating ongoing compliance challenges for PV teams.
02
Safety data, case management, and reporting often span multiple systems and stakeholders.
03
QPPVs and PV teams need clear ownership, audit-ready records, and consistent evidence across reporting, signal management, and risk processes.
RegASK is the Agentic AI Regulatory Operating System for life sciences and consumer products companies. Powered by vertical AI and backed by a global network of 1,800+ regulatory subject matter experts, RegASK helps organizations anticipate regulatory change, assess impact, and orchestrate compliance activities across 160+ markets. By combining agentic AI, expert intelligence, and enterprise governance in a single platform, RegASK transforms fragmented regulatory work into coordinated, audit-ready execution.
Instead of manually monitoring thousands of sources, teams gain actionable insights, prioritized workflows, and the confidence to navigate regulatory complexity with greater speed, control, and consistency.
160+
Territories covered
1,800+
Subject matter experts
Near real-time horizon scanning across 160+ markets, including the EU, US, UK, and Canada, with impact assessments and prioritized alerts. Teams see what is coming before it arrives.
Automated workflows reduce time to market and let your team focus on what matters: strategy.
Open API, MCP, and pre-built connectors, with SSO for Veeva Vault and Esko, unify fragmented data across your regulatory ecosystem.
Regulatory monitoring, document management, full audit trail, and direct access to 1,800+ subject matter experts. Every compliance decision is traceable and defensible.
MEET US THERE
AI & Analytics in PV: Unlocking Predictive Insights for Safer Medicines
Session 1: 9:30 AM – 10:30 AM
Anum brings 13 years of regulatory affairs experience across pharmaceuticals, nutraceuticals, and cosmetics, spanning the GCC, EU, CIS, EAEU, Africa, and Southeast Asia. A GCC Expert and content specialist for RegASK’s Agentic AI platform, she helps compliance teams stay ahead of regulatory change and turn safety data into actionable insights. At GCC Pharmacovigilance Training 2026, Anum will be moderating the opening panel on AI and analytics in pharmacovigilance.
GCC Pharmacovigilance Training 2026 takes place June 24–25 in Dubai, bringing together pharmacovigilance, regulatory affairs, drug safety, and healthcare professionals from across the Gulf region. The program focuses on advancing pharmacovigilance practices through regulatory updates, case studies, digital transformation, and emerging technologies. RegASK joins industry leaders to explore how Agentic AI and regulatory intelligence are helping organizations move beyond reactive compliance toward predictive, data-driven approaches to patient safety and regulatory excellence.
Meet RegASK at GCC Pharmacovigilance Training 2026.
Mövenpick Grand Al Bustan, Dubai
Yes. RegASK connects with tools your team already uses through an open API, MCP, and pre-built connectors — including SSO integrations with Veeva Vault and Esko, fitting into your existing ecosystem without disrupting workflows.
No, RegASK does not replace regulatory professionals. It augments their capabilities and empowers them.
The platform automates manual monitoring, tracks global regulatory changes, and delivers actionable insights so regulatory teams can focus on higher-value work. The result is smarter, faster compliance, powered by both human expertise and intelligent automation.
Instead of spending hours on repetitive compliance tasks, regulatory teams use RegASK to accelerate go-to-market timelines, reduce compliance risk, and make faster, evidence-based decisions.
RegASK supports multilingual and regional regulatory needs.
RegASK’s AI-driven engine offers instant translation in 120+ languages and delivers localized insights tailored to specific markets, including United States, Canada, South America, EU, UK, APAC (Japan, China, South Korea, Australia, Singapore etc) and GCC.
RegASK is GDPR-compliant and certified under internationally recognized standards, including ISO 27001 and SOC 2 Type 2.
All data are encrypted in transit and at rest, access is strictly role-based, and the platform is hosted on secure Microsoft Azure infrastructure.
For Life Sciences clients, RegASK aligns with GxP and other relevant industry-specific security frameworks where applicable.
RegASK eliminates manual regulatory monitoring, fragmented workflows, and slow go-to-market. The platform uses AI-driven regulatory intelligence and agents to:
– Reduce manual work by automating global regulation tracking and change detection
– Stay ahead of changing global regulation
– Cut uncertainties with actionable insights and next-step guidance
– Break information silos by centralizing requirements, evidence, and decisions
– Lower compliance risk and costs through continuous monitoring and audit-ready traceability
– Scale to new markets faster with localized, multi-country coverage
– Improve audit readiness and documentation
Result: faster launches, greater predictability, and regulatory teams focused on strategy instead of repetitive tasks.
TRUSTED BY
Let’s explore how RegASK helps your PV team stay compliant, inspection-ready, and ahead of regulatory change across the GCC.
