Speaker Points – Nordic QAforum 2024

Anna Pontén Engelhardt, Chairperson

• Opening and closing remarks.

Peter Borgå & Emil Schwan, Pharmaceutical Inspectors, Swedish Medical Products Agency
Topic: Inspections of wholesalers

• Common deviations (2021-2024).
• Insights from unexpected inspection findings.

Eva Tollefsen, Norwegian Medicines Agency
Topic: Import of medicinal products into the EES

• Acceptable and unacceptable transactions.
• Regulatory oversight and compliance.

Katja Belt, Finnish Medicines Agency
Topic: The responsibility of MAH in ensuring GMP and GDP compliance

• Key findings from inspections.

Marie Louise Shee, Managing Director, Danish Medicines Verification Organisation (DMVO)
Topic: Updates on FMD and verification systems

• How Denmark approaches FMD.
• Improving quality and compliance across industry and user sides.

Guðrún Selma Steinarsdóttir, Expert, Icelandic Medicines Agency
Topic: Pharmacovigilance and patient safety

• Ensuring compliance in small markets.

Véronique Davoust, Global Supply Quality Operations, Pfizer
Topic: European Shortages Monitoring Platform (ESMP)

• Impact of ESMP on the pharmaceutical industry and supply chain.
• Collaboration opportunities between national authorities and companies.

Thomas Noe Vestergaard Pedersen, Medicines Inspector, Danish Medicines Agency
Topic: Case studies from inspections

• Dicillin-recall: Regulatory and quality perspectives.
• Key inspection findings and guidance updates.

Irene Bøggild, Quality Manager & RP, Novo Nordisk Denmark
Topic: Common supplier management issues in a GMDP environment

• Best practices for managing supplier quality.

Key Takeaways from Nordic QAforum 2024: A Leading Pharmaceutical Conference on Quality Assurance

The Nordic QAforum is recognized as the leading quality assurance forum, providing a platform for professionals to discuss QA best practices, regulatory updates, and industry innovations. As a Nordic pharmaceutical event, this conference brings together experts from the pharmaceutical industry to explore cutting-edge advancements in quality assurance, compliance, and risk management.

Main Themes Covered at Nordic QAforum 2024

🧩 Regulatory Compliance & Best Practices
One of the key discussions at this year’s event focused on regulatory compliance and how organizations can navigate evolving GMP standards, FDA, and EMA guidelines. Experts provided insights into quality systems that align with global regulatory expectations, helping companies stay ahead of industry requirements.

🔬 Pharmaceutical Research & Innovation
This year’s forum highlighted emerging innovations in pharmaceutical research, with discussions on new drug development, quality control improvements, and AI-driven automation in QA. Attendees gained valuable insights into how technology is reshaping pharmaceutical quality assurance, ensuring efficiency, accuracy, and compliance at every stage.

🛠️ Risk Management in Quality Assurance
Effective risk management is at the core of quality assurance best practices. Industry specialists shared strategies for proactively identifying and mitigating compliance risks, reducing errors, and improving overall product safety. Real-world case studies demonstrated the importance of early risk detection and continuous quality monitoring.

🤖 Digital Transformation & AI in QA
As technology advances, AI and automation are becoming integral parts of quality assurance processes. Experts discussed how AI-driven predictive analytics, automated compliance tracking, and digital quality systems are transforming pharmaceutical manufacturing, making QA more efficient and reliable.

🔍 Auditing & Inspections: Ensuring Compliance
Workshops and pharma industry seminars provided deep dives into auditing best practices, including self-inspections, third-party audits, and regulatory compliance checks. Attendees learned how to prepare for and successfully navigate audits, ensuring their organizations meet the highest QA standards.

🌍 Sustainability in Quality Assurance
Sustainability is increasingly important in pharmaceutical manufacturing. This year’s conference featured discussions on eco-friendly quality assurance solutions, highlighting strategies to reduce environmental impact while maintaining compliance with industry regulations.

A Conference That Defined the Future of QA

The pharmaceutical conference program at Nordic QAforum was designed to equip attendees with practical strategies, expert knowledge, and innovative tools to drive excellence in quality assurance.

With a blend of interactive workshops, expert panels, and real-world case studies, this year’s event reinforced its position as the go-to quality assurance forum for professionals in the pharmaceutical industry.

💡 Looking ahead? Stay connected with Nordic QAforum for future quality assurance forums, pharmaceutical conferences, and industry-leading events.

Whether you’re a seasoned professional or new to the field, the Nordic QAforum offers valuable opportunities to enhance your skills and network with peers who are equally passionate about quality assurance. If you are looking for a pharmaceutical conference is this the nordics top choice.

“This forum is a must-attend for anyone serious about Quality Assurance. The knowledge shared here is unparalleled.”

As industries evolve, quality assurance (QA) must also adapt to new technologies, regulations, and challenges. At Nordic QAforum, industry leaders discuss emerging trends that are shaping the future of quality control, regulatory compliance, and risk management.

1. Artificial Intelligence & Automation in QA

The integration of AI-driven analytics, automated compliance tracking, and predictive quality control is transforming pharmaceutical quality assurance. In the coming years, machine learning algorithms will enhance real-time data monitoring, ensuring faster issue detection and resolution.

💡 Example: AI-powered automated inspections are already reducing human error in pharmaceutical manufacturing, ensuring consistent GMP compliance.

2. Blockchain for Data Integrity & Traceability

With growing concerns about data integrity and cybersecurity, many organizations are exploring blockchain technology to ensure tamper-proof records in quality management systems.

🔗 How It Works: Blockchain allows for transparent, immutable documentation of compliance records, which is particularly useful in pharmaceutical supply chain management.

3. The Rise of Sustainability in Quality Assurance

Sustainability is no longer just a trend – it’s a necessity. Companies are shifting towards eco-friendly QA processes, including green manufacturing, waste reduction, and energy-efficient production.

🌱 Future Outlook: Regulatory bodies are introducing new sustainability compliance requirements, making environmental responsibility an essential part of quality assurance programs.

4. Enhanced Risk Management & Predictive Analytics

Instead of reacting to compliance failures, companies are implementing predictive risk management strategies to prevent quality issues before they occur.

📊 Why It Matters: AI-driven analytics and big data help identify patterns and predict potential compliance risks, improving overall product safety and efficiency.

5. Remote & Digital Auditing in a Post-Pandemic World

The shift to remote work and digital operations has led to a rise in virtual audits and cloud-based compliance management systems.

💻 Future Potential: More companies are investing in real-time digital audits to ensure continuous compliance, even in remote settings.

Preparing for the Future of QA

The future of quality assurance will be data-driven, AI-powered, and more globally interconnected than ever before. Attending forums like Nordic QAforum and QAforum Sweden ensures that QA professionals stay ahead of these changes and lead the way in compliance, risk management, and innovation.

🔎 Want to stay updated on the latest trends? Join us at the next Nordic QAforum and QAforum Sweden to gain expert insights and hands-on experience with the latest advancements in quality assurance.

1. What is Nordic QAforum?

Nordic QAforum is the leading quality assurance forum in the Nordic region, bringing together industry experts, researchers, and professionals to discuss best practices, regulatory updates, and emerging trends in quality assurance. The event features keynote speakers, workshops, and networking opportunities, making it an essential conference for those working in quality control, pharmaceutical compliance, and risk management.

2. Where and when does Nordic QAforum take place?

Nordic QAforum is held annually in Denmark. The exact date and location vary each year, and updates are provided on our official website.

3. What is QAforum Sweden?

QAforum Sweden is a separate forum based in Stockholm, Sweden, dedicated to Swedish quality assurance professionals. It provides insights into local regulations, industry developments, and networking opportunities, helping companies comply with Swedish and European quality standards. Learn more at QAforum.se.

4. Who should attend Nordic QAforum?

The event is designed for:
✔️ Quality assurance professionals in pharmaceuticals, biotech, and manufacturing
✔️ Regulatory compliance specialists and GMP/GDP experts
✔️ Auditors, inspectors, and consultants
✔️ Decision-makers and leaders in QA and supply chain management

5. How can I register for Nordic QAforum or QAforum Sweden?

You can register through our official websites:
🔹 Nordic QAforum: Visit nordicqaforum.com
🔹 QAforum Sweden: Visit QAforum.se

6. What topics are covered at Nordic QAforum?

Each year, we cover essential topics, including:
📌 Regulatory compliance (GMP, GDP, FDA & EMA guidelines)
📌 Risk management & auditing best practices
📌 Pharmaceutical research & innovation
📌 AI, automation, and digital transformation in QA
📌 Sustainability in quality assurance

7. Are there networking opportunities?

Yes! Nordic QAforum and QAforum Sweden both provide excellent networking opportunities, allowing professionals to connect, exchange ideas, and build industry partnerships.