Qualio events & webinars

Whether it's in-person, online or on demand, we'd love to meet you! Find below which event suits you best.

Featured events

Qualio Accelerate on-demand sessions. Watch the recordings below.

Welcome to Agentic Compliance for Life Sciences
With Rob. An introduction to agentic compliance and what it means for quality teams day to day.
Watch on-demand

Compliance at the Speed of Development
With Sarah. How Qualio’s agentic platform helps compliance keep up with product development.
Watch on-demand

From audit scramble to always-ready
With Meg & Christian. Five ways AI evolves quality management so audit prep stays continuous.
Watch on-demand

How to Build your AI Governance Guardrails
With Tina & Sumatha. Practical guardrails for AI in quality and compliance.
Watch on-demand

Customer Fireside Chat: Transforming Quality Into an Everyday Habit
Customers share how they turned quality into an everyday habit across their teams.
Watch on-demand

Past events & webinars

QMSR is done. Now what?
March 18, 11:00 AM — 12:00 PM EST
Watch recording

From 20 weeks to 4: AI-powered audit prep for life sciences
January 13, 2026 11-12 ET
Watch recording

How to optimize your medical device risk management with ISO 14971
December 17, 2025 11-12.30 ET
Watch recording

Strategies for Premarket Approval (PMA) success
November 6, 2025 11-12 ET
Watch recording

How to build optimal drug quality with ICH Q10
October 23, 2025 11-12.30 ET
Watch recording

What to expect in the next revision of IEC 62304
October 9, 2025 10-11 ET
Watch recording

AI in medical devices: securing European compliance
September 25, 2025 10-11 ET
Watch recording

Tips & Tricks: Maximizing Forms and Resource Library
August 28, 2025 11:30-12:00 ET
Watch recording

How to master the Medical Device Single Audit Program (MDSAP)
September 10, 2025 11-12.30 ET
Watch recording

Everything you need to know about the FDA QMSR
July 31, 2025 11-12 ET
Watch recording

Internal auditing tips: from beginner to expert
May 22, 2025 10-11 ET
Watch recording

Building a culture of compliance
April 23, 2025 11-12 ET
Watch recording

Arming your life science company for the new year: preparation & challenges for 2025
December 18, 2024 10am - 11.15am ET
Watch recording

Essential strategies for pharmacovigilance and post-market surveillance
November 21, 2024 10am - 11.30am ET
Watch recording

PDA/FDA Joint Regulatory Conference 2024
FDA and Parenteral Drug Association (PDA) will host the 33rd Joint Regulatory Conference to emphasize the role of effective quality systems in ...
Learn more

Quality risk management (ICH Q9): advanced practical applications
Discover how pharma companies can bridge the gap between QRM theory and practice, ensuring that risk management procedures align seamlessly with ...
Watch recording

Beyond Compliance: unlocking therapeutic quality excellence
Lifting pharmaceutical and biotech businesses to new levels of quality management.
Learn more

Medical device risk management: ask the expert
Risk management is a vital and complex component of bringing a medical device to market. Peter Sebelius, founder of Medical Device HQ, joins us to ...
Learn more

How to leverage your QMS to streamline regulatory submissions
Regulatory submissions are an unavoidable fact of life for regulated life science companies - but they needn't be painful or protracted. Learn how to ...
Watch recording

Tips & Tricks: Analytics Best Practices
Join us for our monthly webinar series focused on tips and tricks to help customers get the most out of their Qualio QMS. We will focus on different ...
Watch recording

How to be constantly audit-ready
Audits are a quality professional’s worst nightmare: performance review, school exam, and vital professional milestone all in one. The key to ...
Watch recording

Ensuring quality and compliance: the critical role of validation specialists
Are you concerned about maintaining product quality and meeting stringent regulatory requirements in the rapidly evolving pharma and biotech ...
Watch recording

Taking risks: ICH Q9 quality risk management
How can highly-regulated life science companies confidently spot, address and fix their operational risks? Watch our webinar recording to learn: How ...
Watch recording

.jpg) Medical devices in Europe: busting myths and misconceptions
Cracking the European market for your medical device or in vitro diagnostic device can be a long and complex process. And companies tackling EU ...
Watch recording

How to build a paperless quality management system
Paper adds clutter, chaos, and complication to your quality management system. Last year’s industry initiatives like the GAMP 5 Second Edition and ...
Watch recording

Qualio Tips and Tricks - Document Migrations in Qualio
Watch our monthly webinar series focused on tips and tricks to help customers get the most out of their Qualio QMS. We will focus on different topics ...
Learn more

.png) Qualio Tips and Tricks - All About Training Plans
Watch our monthly webinar series focused on tips and tricks to help customers get the most out of their Qualio QMS. We will focus on different topics ...
Learn more

.png) Medtech post-market essentials
Post-market surveillance planning and reporting is a new motion for many medtech regulatory affairs teams. Unclear and inconsistently enforced ...
Learn more

.png) CSV to CSA: the evolution of digital life science quality
Regulatory agencies and industry bodies like the FDA and ISPE want life science companies to embrace modern, digital tools for stronger supply ...
Learn more

.png) Product update showcase
There are 4 Help Center articles referenced throughout this webinar. Here are the links to those articles. New Editor Functionality Transitioning to ...
Learn more

.png) Keeping up with quality management in a business
Every quality manager wants a connected, collaborative and business-wide culture of quality. But that ambition doesn’t always match reality. ...
Learn more

.png) Integrity of quality and the quality of data integrity
Product quality is fundamental in regulated industries such as the pharmaceutical, food, and cosmetics industries. Furthermore, the proof of quality ...
Learn more

.png) FDA Quality Management Maturity program – what’s new and how to implement
FDA describes Quality Management Maturity (QMM) as the state attained when drug manufacturers have consistent, reliable, and robust business ...
Learn more

.png) Qualio Tips and Tricks - Conducting Effective Management Reviews
Join us for our monthly webinar series focused on tips and tricks to help customers get the most out of their Qualio QMS. We will focus on different ...
Learn more

.png) How to manage your life science suppliers like a pro
Your life science company’s quality and compliance is only as strong as the weakest link in your supply chain. But as supply chains get longer and ...
Learn more

.png) Mastering your 510(k) submission process
Bringing a Class II medical device to the American market? You’ll need to go through the 510(k) process, your gateway to FDA clearance. Yet many ...
Learn more

.png) Ultimate guide to placing a medical device on the UK market
Every medical device start-up dreams of market success and that first influx of revenue. But until you meet UK MDR requirements and register with the ...
Learn more

Ultimate guide to placing a medical device on the EU market
Every medical device start-up dreams of market success and that first influx of revenue. But until you secure EU approval, the vast European market ...
Learn more

.png) How to adapt your QMS to address significant changes and risks
In this webinar, industry insider and QMS expert, Charley Maxwell explains how the QMS is a living, breathing system that needs regular health ...
Learn more

.png) Quality vs. compliance: moving beyond standards
Many regulated businesses chase a baseline of compliance, setting standard accreditation and audit-passing as the primary objective of their quality ...
Watch recording

When's the right time to get an eQMS?
Regulated businesses are realizing the powerful benefits that an eQMS offers. But they don’t always consider how to weave digital quality management ...
Learn more

.png) Getting ready for an audit: how life science companies can prepare
For life science professionals, upcoming audits can be stressful blots on the calendar, which bring last-minute scrambles, sleepless nights and ...
Learn more

.png) Cloud vs. on-premise QMS software: which should I choose?
Summary of Webinar: Quality-conscious life science businesses know they need quality management software to get stronger, fitter and smarter. But as ...
Watch recording

.png) Audits and inspections: how to drive a standardization strategy that sticks
Watch this webinar recording to learn: Why standardization is the key to world class regulatory and quality management How audits and inspections are ...
Watch recording

IVDR compliance: tips and best practice
Watch this webinar to: Learn about the key requirements of the EU's In Vitro Diagnostic Regulation (IVDR) as it comes into effect Understand the key ...
Learn more

Mastering risks and opportunities: tips, tools & techniques
Watch our webinar recording to: Get actionable takeaways to strengthen your risk and opportunity management Access tips, tools and techniques for a ...
Watch recording

Building compliance with an electronic quality management system (eQMS)
Watch this webinar to: Understand the dramatic value and efficiency boosts that timely eQMS implementation unlocks Gain clarity on the myths and ...
Watch recording

Combination products: regulatory approach and cGMP requirements
Watch our webinar to learn: cGMP requirements for the classification of drug-device combination products The common pitfalls drug companies face as ...
Watch recording

What your quality management system needs for ISO and FDA regulation
Watch our webinar recording to: Learn about the 12 pillars of quality management from experts with over 30 years of combined experience Understand ...
Watch recording

Culture of quality webinar
Access our webinar recording to: Learn what a culture of quality really is Unpick what a healthy quality culture and its consequences look like Start ...
Watch recording

Reducing time and cost to market for medical devices
Watch this webinar to: Gain a deeper understanding of each step of the journey to the medical device market Learn from experienced professionals on ...
Watch recording

Integrating data integrity requirements into your QMS
Watch this webinar to: Understand how to embed data integrity by design into your business DNA Compare data integrity to data quality and understand ...
Watch recording

Passing an audit: pro tips from an expert QA panel
Watch our webinar and learn how to: Answer auditors' questions with confidence Deal with findings collaboratively Align the quality team and the ...
Watch recording