Webinars by Industry: Food & Healthcare
Unique Device Identification (UDI)
Unique Device Identifiers (UDI) are mandatory for medical devices and accessories in the U.S. and the EU. They can be found on the device and on packaging. Learn more with our 40-minute on-demand webinar.
Food allergen testing: Frequently asked questions
Food allergy is estimated to affect a staggering 10% of the global population and is on the rise in countries around the world. With rates of prevalence increasing, it’s more important than ever for food businesses to proactively manage their allergen risks. Our panel of experts discuss the issue in our webinar.
Safety Assessment of NIAS and NLS in Food Contact Material in EU
During this webinar, our Pharmacist Toxicologist will explain the requirements applicable for these substances and the toxicological approach needed to ensure the safe use of the plastics containing them.
Webinar: From Screening Methods to Validated Target Methods for Extractables and Leachables Studies
Insight into method development for extractables and leachables studies
Tea Break Webinars: Pesticide Analysis for Tea
A 15 minute webinar providing an overview of pesticide residues and their relevance for tea products, common test methods and more, hosted by Alina Nippes – State Certified Food Chemist.
Tea Break Webinars: Risk-Based Quality Control of Tea
A 15 minute webinar providing insight into quality control aspects of tea including quality testing, contamination, and European legislation, hosted by Alina Nippes – State Certified Food Chemist.
Tea Break Webinars: Labelling Requirements for Tea
A 15 minute webinar providing insight into labelling requirements for the EU, hosted by Katrin Tetens, Head of Testing and Label Validation.
MoCRA Update
The Modernization of Cosmetics Regulation Act (MoCRA) brings forth the first major change to U.S. cosmetics legislation in over 80 years. Join us for an update on MoCRA and how your company can plan to be compliant with its requirements.
On-Demand Medical EMC webinar: “IEC TR 60601-4-2”
Explore our on-demand webinar on IEC TR 60601-4-2, delving into medical device EM immunity guidance by Intertek's Nicholas Abbondante. Understand its scope and testing intricacies in just 12 minutes.
Accessibility Awareness with AccessCheck
Discover how to create an inclusive environment with Intertek's AccessCheck program, ensuring facilities cater to all. Join our webinar to learn about the assessment protocol and take the first step toward inclusivity.
"Bridge to China": Compliance With China's NMPA Requirements
Discover our complimentary on-demand webinar centered on navigating the NMPA regulations governing the export of medical devices to China.
Best Practices in Auditing: Internal Audit
Explore ISO 9001 Auditing Best Practices in our webinar series. Join the upcoming session on Internal Audit Value, where Technical Director Jorge Correa discusses audit processes, risk-based thinking, and utilizing audit insights for continuous improvement in management systems.
Best Practices in Auditing: Statutory and Regulatory Requirements
Join our Best Practices in Auditing webinar series for insights on ISO 9001. Next topic: Statutory and Regulatory Requirements. Technical Director Jorge Correa guides auditors on monitoring, addressing liabilities, and issuing nonconformities. Stay informed for effective audits.
Best Practices in Auditing: Top Management
Join our webinar series on Best Practices in Auditing. Next up: Best Practices in Auditing: Top Management. Learn about auditing processes, interviews, evaluations, and more with Intertek's Technical Director, Jorge Correa.
Best Practices in Auditing: Organizational Knowledge
Learn about Organizational Knowledge in ISO 9001:2015. Join the webinar with Technical Director Jorge Correa, exploring effective management and auditor considerations for evaluating how organizations handle and utilize their collective and individual experiences to achieve objectives.
Analysis of Additives in Polymers: From Simple to Complex Chemistries - On Demand Webinar
Explore the complexities of polymer additives analysis in our on-demand webinar. Discover essential methods for identifying and quantifying additives in raw materials, solid polymers, and composites. Gain insights into the importance of fit-for-purpose analytical techniques for achieving accurate results.
A Revised Guidance Document for EU Health Claim Applications - What you need to know
Discover essential insights into the updated EU Health Claim Applications guidance document. Stay informed on key revisions to navigate the process effectively.
31 Flavors of Vibration Webinar
Explore the diverse "flavors" of vibration testing in our webinar, "31 Flavors of Vibration". From single-axis to multi-axis, and beyond, discover when and why each method is essential for your testing program. Topics include field data replication, acoustic test methods, and more.
Adding Value Through Partnered Customized Audit Services
Discover Intertek's Custom Audit Solutions in our one-hour recorded presentation. Our experts detail how these solutions simplify auditing requirements, offering collaborative and tailored approaches. Learn how customized audits evaluate facilities or suppliers to your specific standards, ensuring quality and mitigating risks to your business and brand.
Webinar: Extractables and Leachables Assessment for Inhalation Drug Products
OINDP product formulations (which is primarily a propellant including an organic solvent) have a high potential for the leaching of substances from the inhalation device components. With a focus on metered dose and other inhalation products, this webinar touches on how extractables/leachables studies can be effectively applied to understand how the formulation interacts with the rubber and plastic inhaler device components to ensure a safe inhalation product.
NetPortal Online Training
Learn about NetPortal and its many web-based capabilities including reviewing live results, production of certificates, and registration of routine samples, among other topics.
Outsourcing Stability Studies to Contract Laboratories; Optimising Success
Join our webinar with expert Kerry Bradford as she shares insights on creating effective stability protocols for outsourced studies, covering critical information, in-house knowledge gaps, and sample handling at contract laboratories to ensure smooth operations.
EMC 4th Edition Basics and Risk Management (RMF) Requirements
The fourth edition of IEC 60601-1-2 includes a number of dramatic changes, including more robust risk analysis requirements. FDA is recommending electromagnetic compatibility (EMC) testing to IEC 60601-1-2 4th Edition standards, requiring manufacturers to submit test plans and risk analysis documents before testing.
Analytical and Mechanical Properties as it Relates to Medical Devices Webinar
Join us for a webinar on how analytical and mechanical characterization drive the development, manufacturing, and failure analysis of medical devices. Led by Paula McDaniel, PhD, Director of Business Development at Intertek Chemical & Pharmaceuticals, explore the critical role of analytical insight in raw material qualification, reverse engineering, residue identification, and material failure analysis. Gain insights and illustrative examples showcasing the importance of testing throughout the product lifecycle.