Professional training · Pharma industry

Regulatory Intelligence: turning constraint into competitive advantage.

A 4-day, 100% practical training — tools, not just theory — designed to make regulatory affairs a lever of performance and strategic decision-making in your organization.

4 days · 9am–5pm · in person In-company Main language: English (FR/AR facilitated) AI integrated
Why this framework exists

Born in complexity. Built for it.

Throughout my career as a Regulatory Affairs expert, structuring regulatory intelligence was one of the hardest problems I faced. I worked in a highly complex environment where regulations are not always clear, and where they change constantly.

Nothing off the shelf worked: international frameworks assumed a stability and transparency our market doesn't have, while local habits relied on individual memory and improvisation.

So I built my own framework — one that fits international practices, but is designed to work in the reality of the Algerian market. That framework is UCIRI, and this training transfers it to your team.

— Rima Belfedhal, creator of the UCIRI framework

Objective

From reactive role to strategic partner

This training repositions regulatory affairs at the heart of company strategy. No more archivist profile: you will learn to turn raw data into decision-oriented intelligence.

01Master Regulatory Intelligence

Turn raw data into actionable insights for the organization.

02Filter & interpret

Extract the relevant signals from regulatory noise to generate usable information.

03Anticipate to act

Adopt a proactive posture toward change and steer the company strategically.

04Reduce risk

Accelerate processes, reduce delays and improve decision quality.

The program's philosophy: Know earlier · Act faster · Decide smarter

The structured framework

UCIRI — 5 steps to rigorous, traceable Regulatory Intelligence

UUnderstand — map the regulatory environment and identify key stakeholders.
CCollect — gather relevant information without overload, from reliable, validated sources.
IInterpret — analyze impact, assess risks and produce actionable conclusions.
RRespond — trigger Change Control, run gap analysis and manage escalations.
IIntegrate — ensure traceability, action tracking and continuous improvement through KPIs.
What you leave with

Concrete tools, immediately deployable

Deliverables included

  • Operational templates: RACI, impact sheet, regulatory monitoring plan — directly usable
  • The complete UCIRI framework, documented and illustrated with real cases
  • Communication models to escalate, report and communicate with decision-makers
  • A 90-day action plan: quick wins, prioritized improvements and follow-up milestones

Pedagogy & approach

  • Interactive and participative — professional exchanges and sector experience sharing
  • Every concept is anchored in a concrete tool or template
  • Immediate applicability — focused on participants' real professional environment
  • AI integrated into Regulatory Intelligence processes
Who is it for

Pharma professionals in Algeria and MENA

Regulatory Affairs Pharmacists

Specialists and managers who want to structure and elevate their regulatory monitoring practice.

Quality Assurance Pharmacists

Quality managers seeking to integrate RI into their compliance and change-management processes.

Technical Directors

Technical directors who want to drive regulatory compliance as a strategic advantage.

Assistant Technical Directors

Assistant pharmacists building skills to support the regulatory transformation of their organization.

The RI toolbox

Tools & resources

Practical tools from the UCIRI framework, published here as they are released. Check back — this library grows.

Coming soon

Regulatory Monitoring Plan template

Structure your regulatory watch: sources, frequency, owners and escalation paths.

Coming soon

Regulatory Impact Sheet

Assess and document the impact of a regulatory change in a single, shareable page.

Coming soon

RACI Matrix for RI

Clarify who is Responsible, Accountable, Consulted and Informed at every UCIRI step.

Your trainer

Rima Belfedhal

Doctor of Pharmacy · Consultant & trainer in Pharmaceutical Regulatory Affairs · Compliance & digitalization specialist. Lean Six Sigma Green Belt certified, applied to regulatory processes. Regulatory Affairs career across Algeria, the Maghreb and Francophone Africa.

Johnson & Johnson GSK Sanofi Lean Six Sigma Green Belt Board Advisor — Health Nexus Africa
Take action

Bring UCIRI into your organization.

In-company sessions, with an optional contextualization day to adapt the program to your laboratory's needs. Guaranteed outcome: a clear method, concrete tools, an immediate action plan.

Request the program & a quote