Upcoming Events & Webinars | Qualio

Upcoming events & webinars

In-person event

Medical device/SaMD

Project Medtech Houston

Nov 19, 2024, 9:00 CT – Nov 20, 2024, 15:00 CT

Essential strategies for pharmacovigilance and post-market surveillance

November 21, 2024 10am - 11.30am ET

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

December 18, 2024 10am - 11.15am ET

Past events & webinars

In-person event

DIA Canada Annual Meeting

Nov 14, 2024 7:30 AM - Nov 15, 2024 4:10 PM

In-person event

Medical device/SaMD

LSI Europe 2024

The LSI Emerging Medtech Summit series is where the most influential medtech & healthtech companies come together in the pursuit of innovation. ...

In-person event

RESI Boston

RESI helps companies gain unprecedented visibility into the early-stage life science community and also leverages Life Science Nation (LSN)’s ...

In-person event

RAPS Convergence 2024

RAPS Convergence is the largest and most recognized annual gathering of global regulatory affairs professionals. Convergence brings together ...

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

Discover how pharma companies can bridge the gap between QRM theory and practice, ensuring that risk management procedures align seamlessly with ...

In-person event

LSX World Congress 2024

The event brings together the CEOs and senior decision makers from the world's most innovative biopharma, medtech and healthtech companies with ...

In-person event

Medical device/SaMD

Project Medtech Midwest Showcase

Showing off the Midwest's Regional Medtech Ecosystem.

Beyond Compliance: unlocking therapeutic quality excellence

Lifting pharmaceutical and biotech businesses to new levels of quality management.

In-person event

Medical device/SaMD

LSI Emerging Medtech Summit USA '24

The must-attend medtech partnering & investment event of 2024 attended by leading medtech startup CEOs and the investors and deal-makers building ...

In-person event

Texas BioLife Summit

A regional gathering of Texas’s leading industry experts in the biotechnology, pharmaceutical, healthcare equipment and services, and related life ...

In-person event

SCBio Annual Conference

Join hundreds of industry leaders, biotech and pharma executives, government and higher education officials, and life sciences supporters from across ...

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 ...

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 ...

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

Audits are a quality professional’s worst nightmare: performance review, school exam, and vital professional milestone all in one. The key to ...

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 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 ...

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 ...

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 ...

Medical device/SaMD

Medical Devices-EU MDR Compliance Webinar

Learn everything you need to know about EU MDR from Jason Jegge, principal consultant at MWA Consulting.

How to evolve from paper to eQMS

Life science quality professionals are turning from their paper-based quality systems in droves. Digital quality management promises stronger ...

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 ...

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 ...

Medtech Post-Market Essentials: Unpacking MDR/IVDR requirements, compliance strategies, and the responsibilities of regulatory and quality teams

Post-market surveillance planning and reporting is a new motion for many medtech regulatory affairs teams. Unclear and inconsistently enforced ...

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 ...

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 ...

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. ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

Qualio Tips and Tricks

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 ...

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 ...

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 ...

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 ...

Qualio Tips and Tricks

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 ...

Medical device/SaMD

Unlocking the British and European markets with UKCA and CE marking

Without a CE mark, or its post-Brexit equivalent the UKCA mark, the pathway between your medical device and millions of potential European and ...

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 ...

A deep dive into our newest integrations

Data and workflow fragmentation is a frustrating and time-consuming issue for quality professionals. At Qualio, we’re working hard to let you bring ...

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 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 ...

How to fund your life science start-up with non-dilutive funding

Watch this webinar to: Gain knowledge about all relevant sources of funding for life science companies Learn about the process for applying Discover ...

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 ...

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

Watch our webinar recording to: Learn about the 12 pillars of quality management from experts with over 30 years of combined experience Understand ...

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 ...

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 ...

Medical device/SaMD

Introducing Qualio Design Controls

Watch this webinar to learn: How Qualio Design Controls eliminates silos between quality and engineering teams by absorbing data from Jira, Azure ...

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

Watch our webinar and learn how to: Answer auditors' questions with confidence Deal with findings collaboratively Align the quality team and the ...

How to maintain and improve your quality management system while working remotely

Watch this webinar to: Learn how to manage, control and optimize your QMS activities from anywhere Access best practice and ideas from quality ...