Resources
Webinars
Recorded sessions and live briefings from USDM and partners.
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Showing 51 of 51 resources
USDM Life Sciences Summit 2026
Watch the 2026 USDM Life Sciences Summit on-demand to learn how to accelerate digital trust, adopt AI safely in GxP operations, modernize TPRM and cybersecurity, and enable the next-gen regulated workforce.
EUDAMED Has Landed – What It Means for You, Now
Watch this on-demand session with Jay Crowley on the EUDAMED mandatory-use milestone: what the first four modules activate, why May 28, 2026 matters, and how to turn MDR/IVDR and UDI data readiness into a practical plan.
EUDAMED Challenges for Medical Device Manufacturers: Future-Proof Your 2025 Compliance Strategy
Watch this on-demand webinar with USDM Life Sciences and BYRD Health to learn how medical device manufacturers can achieve audit-ready EUDAMED and UDI registration before the early-2026 MDR deadlines.
Navigating ICH E6(R3) with Confidence – A New Standard for IT Governance in Clinical Research
Watch this on-demand webinar to see how USDM's CRO Assurance helps sponsors meet ICH E6(R3)'s new continuous IT governance and CRO oversight requirements with confidence.
Smart Strategies for Life Sciences: Leveraging Data for APM Excellence
Watch this on-demand webinar with Blue Mountain and USDM to learn how life sciences teams connect asset, maintenance, and calibration data to improve uptime, defend compliance, and apply AI to asset performance management without losing GxP discipline.
USDM Life Sciences Summit 2025
Watch the USDM Life Sciences Summit 2025 on demand — four expert panels on data integrity, intelligent automation, AI use cases, and strategic technology alliances that turn data into a compliant advantage for regulated life sciences organizations.
Digital Innovation in Life Sciences: Ensure Compliance with Oracle CloudSure
Watch this on-demand webinar to see how Oracle CloudSure, built for life sciences, helps GxP organizations accelerate continuous compliance, reduce SaaS risk, and innovate confidently in the cloud.
Mandatory Use of EUDAMED Now Starting Q1 2026
Watch this on-demand webinar from USDM Life Sciences and BAYARD to understand the EU's gradual EUDAMED roll-out, why mandatory UDI and device registration now starts in Q1 2026, and how to manage your UDI data to meet the deadline.
Ensuring AI Compliance and Maximizing the Value of Your GxP Technologies
Watch this on-demand webinar with Google, Sorcero, and USDM on how a purpose-built, compliant AI solution helps life sciences organizations adopt AI responsibly and mitigate risk across GxP technologies.
USDM Life Sciences Summit 2024
Watch the USDM Life Sciences Summit 2024 on demand: a three-session event on the state of AI in life sciences — covering the GxP regulatory landscape, practical AI use cases for workflow automation, and a governance framework for compliant, responsible AI adoption.
Automate Now | Best Practices for GxP Systems
Watch this on-demand webinar with USDM subject matter experts on best practices for GxP systems—covering automated testing, IT change management, and AI to decrease risk and increase operational efficiency.
Integrated GxP Compliance
Watch this on-demand webinar to see how USDM Integrated GxP Compliance—a modern managed service—helps pharma, biotech, and medical device companies harmonize compliance with technology, automate validation, and accelerate innovation across cloud and on-premises GxP systems.
An Update on the FDA’s UDI and GUDID Compliance Requirements
On-demand webinar with Jay Crowley on the FDA’s tightening UDI and GUDID requirements — closing Legacy Identifier gaps, UDI in routine inspections and import screening, and how labelers can align GUDID data across FDA systems before enforcement reaches them.
Managing GxP Workflows & Continuous Cloud Compliance with ProcessX and ServiceNow
Watch this on-demand webinar to see how ProcessX on ServiceNow helps life sciences teams automate GxP and non-GxP workflows, preserve 21 CFR Part 11 controls, and scale regulated processes in a state of continuous compliance.
Simplify GxP Quality Assurance
On-demand webinar: ZenQMS and USDM Life Sciences show how to simplify selecting, qualifying, and validating cloud-based eQMS systems for GxP — and how Cloud Assurance reduces your validation burden.
NetSuite for GxP, Regulated Use Cases
Watch this on-demand webinar to see how life sciences organizations use NetSuite for GxP-regulated processes — from item and material management to 21 CFR Part 11 e-records, audit trails, and e-signatures — and how USDM reduces the compliance burden.
Emerging Life Sciences Virtual Event
Watch this on-demand virtual event, hosted by USDM Life Sciences with Box, for thought-leader guidance on IT and quality strategy, GxP cloud compliance, automation, and compliant content management as emerging biotech, biopharma, and medical device companies move from R&D to commercialization.
USDM Life Sciences Summit 2023
Watch the on-demand USDM Life Sciences Summit 2023: an FDA Computer Software Assurance (CSA) update, a prescriptive approach to automated GxP cloud compliance, real customer cloud-journey case studies, and a panel on progressive life sciences technology.
Compliant IT Strategies On-Demand Webinar
Watch this on-demand webinar to build a compliant IT strategy for early-stage biotech, pharma, and medical device companies—from pre-clinical through commercialization—covering IT roadmaps, GxP and G&A needs, cybersecurity, and scalable resourcing models.
Computer Software Assurance (CSA) Draft Guidance Webinar
Watch this on-demand webinar with the FDA's Francisco Vicenty and USDM experts as they break down the Computer Software Assurance (CSA) Draft Guidance and what the shift from traditional CSV means for medical device, pharma, and biotech organizations.
UDI Beyond Borders
Watch the on-demand 12th annual UDI Conference, moderated by Jay Crowley — the original developer of the FDA's UDI requirements — for a global look at FDA, EU MDR/IVDR, and emerging international Unique Device Identification rules, plus the data quality and data management practices device manufacturers need to comply.
Global UDI Data Management – The New Paradigm
Watch this on-demand webinar on managing Unique Device Identification (UDI) data across the growing set of national UDI databases — from data mapping and transformation to maintaining continuous compliance with USDM Cloud Assurance for atrify.
Automating Validation Across Your Tech Stack
On-demand webinar: USDM experts walk through a forward-thinking approach to automating computer system validation and continuous compliance for modern GxP cloud technologies—so you can deploy faster without choosing between regulation and innovation.
Demystify FDA Compliance for Public Cloud Workloads in Life Sciences
Watch this on-demand expert roundtable from USDM Life Sciences and Data Intensity on adopting public cloud for FDA-regulated workloads while keeping GxP applications secure and compliant.
Cannabis: Compliance in a Rapidly Changing Industry
Watch this on-demand webinar to understand the fragmented cannabis regulatory landscape, get a regulations and compliance overview, and learn from real FDA findings so you can prepare your company for evolving requirements.
Challenges with EU MDR and IVDR Compliance
Watch this on-demand webinar on EU MDR and IVDR compliance for medical device manufacturers — EUDAMED data requirements, UDI strategy, and the steps to take now to meet upcoming and future global deadlines.
EU MDR Date of Application Readiness
Watch this on-demand webinar for near-term and long-term EU MDR Date of Application (DoA) strategies — covering Directive, Legacy, and Regulation device requirements, EUDAMED timing, and the transitional deadlines running through 2025.
Evolving Global UDI Product Data Requirements
Watch this on-demand webinar on evolving global UDI requirements, where former FDA UDI architect Jay Crowley and atrify's Lionel Tussau explain how medical device manufacturers can manage regulatory, commercial, and patient-safety product data across EUDAMED, GDSN, and other global systems.
How to Get Results on Regulated Projects with Virtual Teams
Watch this on-demand USDM webinar for a practical playbook on running regulated GxP projects with virtual, distributed teams — covering virtual PMO best practices, compliant collaboration tools, common mistakes to avoid, and how to maintain business continuity and continuous compliance.
How to Comply with Saudi Arabia UDI Requirements
Watch this on-demand webinar to understand SFDA Unique Device Identification (UDI) requirements for medical devices and IVDs in Saudi Arabia, including SAUDI-D database submissions, labeling, and compliance deadlines by device class.
How to Maximize Your GxP Use of the Public Cloud
Watch this on-demand webinar to learn how life sciences teams scale GxP workloads in the public cloud while maintaining continuous compliance across IaaS, PaaS, and SaaS based on their cloud maturity.
SaMD Regulations and Compliant Development Environments
Watch this on-demand USDM webinar on Software as a Medical Device (SaMD): the U.S. and European regulations that apply, QMS considerations, and how to build a compliant, qualified IT development environment.
UDI Registration in EUDAMED – Why and How to Use It Now
Watch this on-demand webinar to learn how to register devices in EUDAMED's new UDI Database module, navigate MDR actor registration, and prepare for EUDAMED's future steps.
Virtual Audits and Inspections
Watch this on-demand webinar with USDM Life Sciences and Box to see how virtual audits streamline vendor and supplier qualification, support agency submissions, and keep records accessible for remote regulatory inspections.
Work Faster and Smarter in Biotech Quality Management
Watch this on-demand webinar to see how Box, ComplianceQuest, and USDM Life Sciences bundle quality management so biotechs cut stand-up times, control costs, and run a best-of-breed compliance stack.
An Introduction to Computer Software Assurance
Watch this on-demand webinar with USDM's Sandy Hedberg for a plain-language introduction to the FDA's Computer Software Assurance (CSA) approach — what it means for regulated life sciences companies and how this risk-based alternative to traditional CSV can be applied to your IT systems today.
Cybersecurity Threats and Risks to Life Sciences Companies
Watch this on-demand webinar to understand the current and emerging cybersecurity threats facing life sciences companies and their third-party providers, and how to evaluate and manage risk to protect intellectual property, data, patient privacy, and continuous regulatory compliance.
Oracle Validation and Assurance Virtual Roundtable
Watch this on-demand roundtable with USDM Life Sciences and Oracle on validating Oracle Cloud for life sciences — covering the FDA's Computer System Assurance (CSA) guidance, Oracle SCM, and USDM Cloud Assurance to reduce compliance costs.
Update from the FDA on CSV Changes
Watch this on-demand webinar with the FDA's Francisco Vicenty and USDM's Sandy Hedberg to understand the shift from Computer System Validation (CSV) to the risk-based Computer Software Assurance (CSA) approach — and how to apply it to your regulated systems today.
Tips for Start-Ups: How to Build a Cohesive, Integrated QMS
Watch this on-demand USDM webinar for emerging life sciences companies on building a cohesive, integrated Quality Management System (QMS) — a top-down framework aligned to ICH Q10, ISO, and FDA expectations that closes the gaps regulators find first.
Accelerate Your Journey to the Cloud: Move your GxP Regulated Workloads to Microsoft Azure
On-demand webinar with Microsoft and USDM Life Sciences on accelerating the migration of GxP regulated workloads to Microsoft Azure using USDM’s Cloud Assurance — covering the shift from CSV to a continuous, risk-based compliance model across IaaS, PaaS, and SaaS.
Q&A with the FDA on CSV Changes
On-demand Q&A webinar with the FDA's Francisco Vicenty and USDM's Sandy Hedberg answering life sciences industry questions on CSV changes and Computer Software Assurance (CSA).
Accelerating Cloud Content Management for Emerging Life Sciences
On-demand webinar: how pre-commercial and newly commercialized life sciences companies can adopt a cloud-first approach to regulated content management, choose the right vendor, and stay GxP compliant in the public cloud as they scale.
IT Systems for Emerging Life Sciences – from R&D to Commercial
Watch this on-demand webinar to learn how emerging life sciences companies move from paper to the cloud, automate GxP processes, and build scalable IT systems that carry them from R&D through commercialization while controlling cost and compliance risk.
Seamless Content, Quality, and Compliance in the Cloud
Watch this on-demand webinar to see how life sciences companies unify content, document, training, and change management in one cloud platform while maintaining continuous GxP compliance with USDM's Unify Compliance Cloud.
Reimagining Medical Device Post-Market Surveillance
Watch this on-demand webinar to learn how medical device manufacturers can move post-market surveillance from a passive, complaint-driven activity to a proactive system that meets evolving global requirements and delivers better clinical and safety data.
Your IT Roadmap – Guidance for Early-Stage Life Sciences Startups
Watch this on-demand webinar to build a strategic IT roadmap for your early-stage life sciences company — aligning G&A and GxP functional needs, planning for compliance, and adapting as regulations, technologies, and business requirements evolve.
Oracle Clinical One: Next Generation Clinical Trials with Continuous GxP Compliance
Watch this on-demand webinar to see how Oracle Clinical One unifies clinical trial data, people, and processes on one eClinical platform — and how USDM Cloud Assurance keeps that environment validated and in continuous GxP compliance.
An Introduction to Computer System Validation
Watch this on-demand webinar for a clear introduction to Computer System Validation (CSV) in life sciences — what it is, why the FDA and global health authorities require it, which GxP systems it applies to, and how to plan an audit-ready CSV approach.
Minimize Risk and Maintain Compliance on Veeva with USDM Cloud Assurance
Watch this on-demand webinar to learn how USDM certified Veeva experts keep your Veeva GxP systems in a validated state with Cloud Assurance and modernize your CSV approach using the FDA's computer software assurance (CSA) methodology.
Simplifying Regulated, GxP Business Processes in ServiceNow
Watch this on-demand webinar to see how ProcessX, an intelligent, fully validated GxP process automation platform Built on Now, helps pharma, biotech, and medical device companies automate regulated business processes in ServiceNow while staying in a continuous state of validation.