Quality That Works: Pragmatism Over Perfection

Safety, Risk, and Pragmatic Compliance — Pharmacovigilance

Join senior QA leaders, compliance specialists, and regulators for three days of practical insights that transform inspection readiness into a competitive advantage. Stop chasing theoretical perfection and start implementing quality that genuinely works.

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Expert-Led Sessions Addressing Your Most Pressing Challenges

1

Risk-Based Training in PV

Day 2, 11:00 (45 minutes)

Unlock inspection readiness with pragmatic, risk-proportionate training approaches. This session equips you to effectively assess training needs, develop impactful content, evaluate competency, and monitor compliance, ensuring your strategies are confidently presented to inspectors and yield tangible results.

2

Key Considerations for the PV Audit Report

Day 2, 15.30 (30 minutes)

Gain a practical understanding of PV audit reporting, from effectively determining and presenting findings to navigating categorisation and proposed actions. This session will equip attendees with pragmatic strategies to assess and structure audit findings and reports tailored to their unique organisational setup, ensuring maximum impact.

3

The QA Interview

Day 3, 08:45 (30 minutes)

Gain critical insights: Discover precisely what PV QA aspects are scrutinised during inspections, anticipate key questions, and master the essential preparation steps to ensure readiness and confidence.

Why Attend the Safety, Risk, and Pragmatic Compliance — Pharmacovigilance sessions?

1

Stay ahead of evolving PV compliance expectations

Understand how global regulators and industry peers are redefining inspection priorities and safety oversight.

2

Strengthen your organisation’s risk management

Gain practical approaches to streamline safety processes, reduce reporting bottlenecks, and apply proportional, risk-based methods.

3

Enhance patient safety outcomes

Explore pragmatic strategies that balance compliance with efficiency, ensuring your PV frameworks support faster, safer access to medicines.

Connect with Industry Leaders

The RQA conference offers unparalleled networking opportunities with senior decision-makers who face the same challenges you do. Move beyond theoretical discussions to practical problem-solving with peers who understand your regulatory landscape.

Welcome Reception

Begin forging valuable connections from day one at our exclusive Welcome Reception. Meet speakers, regulators and fellow attendees in a relaxed environment designed to facilitate meaningful conversation.

VIP Networking Sessions

Participate in structured networking roundtables focused on specific compliance challenges. These facilitated discussions ensure you connect with precisely the right people to address your most pressing concerns.

Evening Socials

Continue conversations in a more informal setting at our evening social events. These gatherings have historically sparked collaborative initiatives and valuable professional relationships that extend far beyond the conference.

Who You'll Meet

The RQA conference attracts a diverse yet focused group of professionals responsible for quality assurance and regulatory compliance across pharmaceutical companies, CROs, biotechnology firms, and regulatory bodies.

2024 RQA Conference Attendees Per Continent


Quality Assurance Directors

Senior QA leaders responsible for organisational quality strategy, inspection readiness, and regulatory relationships. Connect with peers facing similar strategic challenges and resource constraints.

Compliance Specialists

Professionals tasked with implementing GxP compliance programmes and preparing for regulatory inspections. Exchange practical approaches to maintaining compliance without operational disruption.

Regulatory Professionals

Representatives from regulatory bodies and professionals managing regulatory affairs within organisations. Gain insight into evolving regulatory expectations and interpretation of guidelines.

Auditors

Internal and external auditors seeking to enhance their audit approaches and effectiveness. Discover methods to add genuine value through the audit process rather than simply identifying deficiencies.

Secure Your Place Today

Attendance at the conference is limited to ensure meaningful interaction with speakers and fellow delegates.

400

Maximum Delegates

Limited places to ensure quality discussions and networking opportunities

70+

Expert Speakers

Senior practitioners and regulators with proven practical experience

9 out of 10

Satisfaction Rate

Previous attendees who would recommend to colleagues


Have questions? Contact our team at conferences@therqa.com.