Events and webinars

Discover how to structure data, avoid common pitfalls, and improve decision-making with real-life examples, led by Kurt In Albon and Àngel Buendía.

Discover how a unified eQMS can ensure GMP compliance while fueling continuous improvement and strategic growth in life sciences.

Explore how a harmonized QMS streamlines operations by aligning quality processes, minimizing risks, and eliminating redundant costs.

Join Matin King as he guides you through implementing AI GPT models in QMS to enhance quality, minimize risks, and drive innovation while ensuring regulatory compliance.

Join Àngel Buendía and Lesley Worthington as they guide you through embedding quality into every aspect of your organization and building a robust quality culture.

Discover how Scilife’s Smart QMS streamlines compliance, enhances document control, and fosters a proactive quality culture under the new IVDR regulations.

Discover how Scilife’s Smart QMS transforms CAPA management by streamlining workflows, fostering collaboration, and enabling agile corrective and preventive actions.

Discover how a Smart QMS helps monitor training progress, ensure compliance and traceability, and automate onboarding, training, and role transitions.

Discover how a Smart QMS streamlines discrepancy recording, simplifies procedure management, and empowers your workforce with essential equipment maintenance skills.

Join Joseph Turton as he explores how critical thinking enhances regulatory navigation, ensures data integrity, and addresses CSV challenges, offering practical techniques for integration into validation processes.

Discover how Scilife’s smart QMS helps medical device companies navigate the new FDA QMSR and align with ISO 13485, ensuring compliance and improving efficiency with a real industry example.

Discover how Scilife’s smart QMS simplifies audit management, turning internal audits into an opportunity for continuous improvement while reducing time and effort.

Discover how Scilife’s Document Control solution simplifies document management, customizes approval workflows, and maintains a clear audit trail with a real-world example.

Watch Rodrigo Nasif discuss the critical synergy between quality and regulatory compliance, sharing practical strategies and real cases to optimize processes and make informed decisions.

Discover how Scilife eQMS improves document management, protects data integrity, enhances audit management, and supports ISO 13485 certification readiness with a real-world example.

Discover how Scilife’s Change Control Management solution helps evaluate, approve, and implement changes to meet regulatory updates, drive continuous improvement, and adapt to new technologies with a real-world example.

Discover how Scilife’s Print & Reconciliation solution ensures data integrity and compliance with 21 CFR Part 11 by using barcode systems and setting up an approved printer network for print control.

Only available for registrants

In this webinar, Evgeniya Makarova enlightened us with the introduction of the Smart Quality approach, a new way of understanding Quality that involves automated and digitized processes and procedures, design-thinking, artificial intelligence, and advanced analytics, to empower a Quality and Continuous Improvement culture. 

1_Challenges of being the first

2_Regulatory requirements of new market opportunities

3_Merging cannabis agriculture with pharma industry

4_Live Q&A session

With Vanessa Vankerckhoven,
CEO and co-founder of Novosanis

1_Go-to-market strategy

2_How to get ISO 13485 certified

3_Quality management in pre-market and post-market phases

4_Pre-acquisition vs post-acquisition

With Amanda Amell 

Enjoy the expertise of Amanda Amell, QA expert at Shoebox, who will explain the Continuous Improvement Framework, the main challenges and the Shoebox case study.

With Amazon (AWS)

We’re thrilled that Patrick Lamplé, the expert on data security in the life sciences sector at Amazon Web Services (AWS), joined Filip Heitbrink in this webinar to share his valuable insights on the subject.

New Scilife features

Our CEO Filip Heitbrink explains how these two handy modules can help you set up a fully compliant Document Control system and training matrix for your team.

With Yves Dène

An interactive Q&A webinar with Yves Dène, Knowledge Manager at QbD, that answers all your questions about how to reach an embedded quality system and ensure data integrity.

with Lučka Bibič

In this Q&A session with Lučka Bibič, you’ll discover how gamification can be used to improve quality within the Life Sciences, how scientific research was turned into a VR game, and how women can overcome the challenges they face in science and tech. 

Watch Andrés Gola, Senior Consultant at PBSV, tackle top regulatory audit questions — from pre-inspection prep to post-audit compliance and future trends.

Learn how to gain buy-in for quality initiatives using soft skills, influence principles, and stakeholder alignment, with insights from Lesley Worthington and Àngel Buendía.

Discover how to structure data, avoid common pitfalls, and improve decision-making with real-life examples, led by Kurt In Albon and Àngel Buendía.

Learn how to spot improvement opportunities, boost cross-functional collaboration, and drive impactful results with insights from Àngel Buendía and Didier Giffroy.

Learn key communication techniques from Kathy Walsh to position compliance as a business priority and align it with organizational goals to gain leadership support.

Join Matin King as he guides you through implementing AI GPT models in QMS to enhance quality, minimize risks, and drive innovation while ensuring regulatory compliance.

Join Àngel Buendía and Lesley Worthington as they guide you through embedding quality into every aspect of your organization and building a robust quality culture.

Join Àngel Buendía and Angela Bazigos as they discuss SaaS eQMS validation, covering GaMP5 compliance, deliverables, and the roles of your company and the vendor.

Gain expert insights into effective pharmaceutical supply chain auditing, covering stakeholder roles, auditor qualifications, and case studies on GMP, GDP, and more.

Join Dr. Kathy Walsh for a practical guide on turning QMS documents from a liability into a plain language asset using a clear writing framework that boosts document quality.

Join Joseph Turton as he explores how critical thinking enhances regulatory navigation, ensures data integrity, and addresses CSV challenges, offering practical techniques for integration into validation processes.

Watch Rodrigo Nasif discuss the critical synergy between quality and regulatory compliance, sharing practical strategies and real cases to optimize processes and make informed decisions.

In this free training, the experts will delve into auditing best practices and key soft skills through four case studies to gain comprehensive knowledge to nail your upcoming audits.

Recent Warning Letters and inspection findings continue to highlight recurring quality and compliance issues. In this CaseLab, Antiksha Joshi explores what these findings can teach us about audit readiness and what organizations can do now to prepare for 2027.

Scaling in DACH? Don’t let disconnected quality systems slow you. Discover how biotech companies can stay inspection-ready with a scalable eQMS approach.

When UK life sciences companies expand into the EU, quality management becomes more complex. This CaseLab explores how to maintain control, compliance, and efficiency across teams, partners, and regulations while scaling internationally.

Many pharma QMS setups are compliant, but manual processes and disconnected systems can still slow performance and growth. This CaseLab explores how a connected digital approach helps reduce hidden costs and improve efficiency.

In this first CaseLab session, independent CSV expert Joseph Turton, together with part of the Scilife team, explored a more practical, risk-based approach to validation—one that shifts the focus from document checklists to credible evidence.

Disconnected tools, manual workarounds, and constant firefighting create a risky pattern: we’ll fix it later. But later rarely comes. In this session, we'll explore why Quality teams fall into this cycle, and how leading organizations shift to sustainable, scalable systems that support growth.

In this showcase we'll show you how Scilife’s KPIs give quality teams real-time insight, so they can anticipate issues instead of reacting to them. 

Regulators now use AI to assess quality and compliance. Learn how to lead digital transformation, ensure data integrity, and meet evolving FDA and EU MDR expectations.

Simplify GxP documentation and training: discover how Scilife's Document Control and Trainings solution reduce manual work, ensure compliance, and streamline audit readiness.

Still chasing CAPAs by email? That mistake could cost you your next audit — or worse. Explore a real-world CAPA use case and see how Scilife turns reactive firefighting into an automated process.

Explore how CDMOs can stay consistently audit-ready, meet sponsor expectations, and gain a competitive edge by shifting from fragmented, manual systems to an integrated eQMS like Scilife.

Still using spreadsheets and inboxes for compliance? You're exposed to hidden risks. Join our webinar to discover how an eQMS like Scilife eliminates manual gaps with full control and traceability.

Tired of complex risk management? In this webinar, our experts walk you through a real use case — a risk assessment of document control in a paper-based system.

Discover how Scilife eQMS improves document management, protects data integrity, enhances audit management, and supports ISO 13485 certification readiness with a real-world example.

Discover how a unified eQMS can ensure GMP compliance while fueling continuous improvement and strategic growth in life sciences.

Explore how a harmonized QMS streamlines operations by aligning quality processes, minimizing risks, and eliminating redundant costs.

Discover how Scilife’s print and reconciliation solution maintains data integrity, automates document tracking, and ensures compliance in paper-based GMP workflows.

Discover how Scilife’s events solution helps manage deviations, strengthen quality culture, and drive continuous improvement in your QMS.

Discover how Scilife’s change control solution streamlines change management in regulated industries, with a real case on resolving a daily calibration issue.

Implementing a solid complaint management system directly impacts the safety of your IVD during post-market surveillance!

Discover how Scilife’s Smart QMS streamlines compliance, enhances document control, and fosters a proactive quality culture under the new IVDR regulations.

Discover how Scilife’s Smart QMS transforms CAPA management by streamlining workflows, fostering collaboration, and enabling agile corrective and preventive actions.

Descubre cómo la transformación digital puede mejorar la eficiencia, reducir costes y asegurar el cumplimiento normativo en la gestión de calidad.

Discover how a Smart QMS helps monitor training progress, ensure compliance and traceability, and automate onboarding, training, and role transitions.

Discover how a Smart QMS streamlines discrepancy recording, simplifies procedure management, and empowers your workforce with essential equipment maintenance skills.

Discover how Scilife’s smart QMS helps medical device companies navigate the new FDA QMSR and align with ISO 13485, ensuring compliance and improving efficiency with a real industry example.

Discover how Scilife’s smart QMS simplifies audit management, turning internal audits into an opportunity for continuous improvement while reducing time and effort.

Discover how Scilife’s document control solution simplifies document management, customizes approval workflows, and maintains a clear audit trail with a real-world example.

This showcase shows how to create a quality management review report, how Scilife simplifies the process, and how to streamline your QMR with practical guidance.

Discover how Scilife’s change control management solution helps evaluate, approve, and implement changes to meet regulatory updates, drive continuous improvement, and adapt to new technologies with a real-world example.

Discover how Scilife’s print and reconciliation solution ensures data integrity and compliance with 21 CFR Part 11 by using barcode systems and setting up an approved printer network for print control.

In this free session, you’ll see a real-world example of how Scilife Smart QMS works. You'll learn how to implement the GDP principles, rules, and criteria in your quality management system. 

In this free session, you’ll see how Scilife’s equipment management software works in practice and how it helps streamline maintenance and calibration with recurring task management.

In this free session, you’ll see how Scilife’s print and reconciliation solution works, how to use the barcode system, and set up an approved printer network to ensure print control and data integrity.

In this free session, you’ll discover the main errors in cGMP environments and a use case of how to avoid inadequate deviation investigations and poor root cause analysis with Scilife. 

In this free session, you’ll see how Scilife’s audits management software works, how to handle audit processes, and how to mitigate findings by linking them to CAPAs, quality events, or change management.

Discover how Scilife helps you implement GLP rules and criteria in your quality management system, simplifying compliance and guiding you through every step.

Discover how Scilife’s Smart Quality Platform can revolutionize your organization's digital capabilities and improve productivity!

Discover how Scilife can improve your clinical trial processes and help you succeed in your sponsor's audit!

Go live with your eQMS faster and with confidence! In this final session of the eQMS Series, we’ll walk you through the whole process, from first steps to full deployment. You’ll hear lessons learned from real-world cases, best practices, and tips to help you go live confidently.

In this 4th eQMS Series edition, you’ll learn practical, risk-based approaches aligned with GAMP 5 2nd Edition, what validation really entails, which activities fall under your responsibility, and how to approach updates and documentation without the stress.

You are considering switching to an eQMS, but importing all of your existing documents into it is already haunting your dreams? Join us to learn how to plan to confidently and successfully handle this transition.

Choose the right eQMS from the start! Learn when to upgrade, what to look for, and how to define your URS—with expert tips and real-life insights from the life sciences field.

If you are considering switching from paper to an eQMS, but are dreading the thought of transferring all of your existing documentation, this webinar is for you!

Simplify design control and ensure product quality from the start with Scilife’s Design and Development.

Discover how Smart Quality empowers Life Sciences organizations to increase productivity and speed in Quality Assurance processes by up to 40% and reduce the total Cost of Quality by up to 50%!