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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.

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Featured events

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

Past events & webinars

QMSR is done. Now what?a
Webinar

QMSR is done. Now what?

March 18, 11:00 AM — 12:00 PM EST
AI webinar promo
Webinar
Regulatory

From 20 weeks to 4: AI-powered audit prep for life sciences

January 13, 2026 11-12 ET
ISO 14971 webinar
Webinar
Medical device/SaMD

How to optimize your medical device risk management with ISO 14971

December 17, 2025 11-12.30 ET
PMA webinar promo
Webinar
Medical device/SaMD

Strategies for Premarket Approval (PMA) success

November 6, 2025 11-12 ET
ICH Q10 webinar promo
Webinar
Pharmaceutical

How to build optimal drug quality with ICH Q10

October 23, 2025 11-12.30 ET
IEC 62304 webinar
Webinar
Medical device/SaMD

What to expect in the next revision of IEC 62304

October 9, 2025 10-11 ET
DQS AI webinar email
Webinar
Medical device/SaMD

AI in medical devices: securing European compliance

September 25, 2025 10-11 ET
Tips and Tricks Webinar
Webinar
Life sciences

Tips & Tricks: Maximizing Forms and Resource Library

August 28, 2025 11:30-12:00 ET
MDSAP webinar
Webinar
Medical device/SaMD

How to master the Medical Device Single Audit Program (MDSAP)

September 10, 2025 11-12.30 ET
FDA QMSR webinar
Webinar
Medical device/SaMD

Everything you need to know about the FDA QMSR

July 31, 2025 11-12 ET
Internal auditing webinar Qualio Medical Device HQ
Webinar
Medical device/SaMD

Internal auditing tips: from beginner to expert

May 22, 2025 10-11 ET
Culture of compliance event
Webinar
Quality culture

Building a culture of compliance

April 23, 2025 11-12 ET
Arming Your Life Science Company for the New Year Preparation Challenges for 2025 Qualistery 300x300 event
Webinar
Regulatory

Arming your life science company for the new year: preparation & challenges for 2025

December 18, 2024 10am - 11.15am ET
webinar Essential Strategies for Successful Pharmacovigilance and Post Market Surveillance 1 1
Webinar
Regulatory

Essential strategies for pharmacovigilance and post-market surveillance

November 21, 2024 10am - 11.30am ET
PDAFDA 2024 event
In-person event
Medical device/SaMD

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 ...
Quality Risk Management ICH Q9 Advanced Practical Applications 2 event
Webinar
Pharmaceutical

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 ...
Beyond Compliance event
Virtual event
Pharmaceutical

Beyond Compliance: unlocking therapeutic quality excellence

Lifting pharmaceutical and biotech businesses to new levels of quality management.
Screenshot 2023 10 04 at 10.55.30 event
Virtual event
Medical device/SaMD

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 ...
Screenshot 2023 09 26 at 08.56.38 event
Webinar
Regulatory

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 ...
using qualio for management reviews event
Webinar
eQMS

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 ...
How to Be Constantly Audit Ready event
Webinar
eQMS

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 ...
Screenshot 2023 07 05 at 16.33.45 event
Webinar
Regulatory

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 ...
Taking risks ICH Q9 R1 quality risk management banner 1 event
Webinar
Pharmaceutical

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 ...
Ultimate guide to placing a medical device on the EU market — Webinar invite templates (1)
Webinar
Medical device/SaMD

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 ...
evolve to a paperless eQMS event
Webinar
eQMS

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 ...
datasheet document management event
Virtual event
eQMS

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 ...
Copy of Website — Webinars Events (24)
Virtual event
Regulatory

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 ...
Copy of Website — Webinars Events (23)
Virtual event
Regulatory

Medtech post-market essentials

Post-market surveillance planning and reporting is a new motion for many medtech regulatory affairs teams. Unclear and inconsistently enforced ...
Copy of Website — Webinars Events (22)
Virtual event
Regulatory

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 ...
Copy of Website — Webinars Events (21)
Virtual event
Regulatory

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 ...
Copy of Website — Webinars Events (20)
Virtual event
Regulatory

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. ...
Copy of Website — Webinars Events (19)
Virtual event
Regulatory

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 ...
Copy of Website — Webinars Events (18)
Virtual event

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 ...
Copy of Website — Webinars Events (17)
Virtual event

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 ...
Copy of Website — Webinars Events (15)
Virtual event
Regulatory

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 ...
Copy of Website — Webinars Events (14)
Virtual event
Regulatory

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 ...
Ultimate guide to placing a medical device on the EU market — Webinar invite templates (1)
Virtual event
Medical device/SaMD

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 ...
Ultimate guide to placing a medical device on the EU market — Webinar invite templates
Virtual event
Medical device/SaMD

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 ...
Copy of Website — Webinars Events (13)
Virtual event
Regulatory

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 ...
Copy of Website — Webinars Events (12)
Webinar
Quality culture

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 ...
icon right time eqms event
Virtual event
Regulatory

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 ...
Copy of Website — Webinars Events (11)
Virtual event
Regulatory

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 ...
Copy of Website — Webinars Events (8)
Webinar
eQMS

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 ...
Copy of Website — Webinars Events (5)
Webinar
Regulatory

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 ...
webinar ivdr
Virtual event
Medical device/SaMD

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 ...
mastering risks event
Webinar

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 ...
building compliance with an electronic quality management system e qms event
Webinar
eQMS

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 ...
sponsored webcast combination products regulatory approach and c gmp requirements event
Webinar
Regulatory

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 ...
what your quality management system needs for iso and fda regulation event
Webinar
Regulatory

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 ...
culture of quality webinar
Webinar
Quality culture

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 ...
reducing time and cost to market for medical devices v2 event
Webinar
Medical device/SaMD

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 ...
integrating data integrity requirements event
Webinar
Regulatory

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 ...
passing an audit pro tips from an expert qa panel event
Webinar
Regulatory

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 ...