The New CFSA Data Guidance for GMM Novel Food Ingredients and Food Additives

This webinar will walk participants through these updated requirements to help ensure compliance.

Navigating EUDR Compliance

The EU Deforestation Regulation will be coming into effective and will impact the import and export of seven commodities to and from the European Union.

Safe Use of Cosmetic Packaging in Europe

This webinar will present the latest applicable guidelines for the safe use of cosmetic packaging in the EU.

Assessing Environmental Hazards in Cosmetic Formulations

This webinar will allow you to understand how to assess the environmental hazards of substances in your formulations, in compliance with EU regulations.

International Cosmetics Regulations

Whether you are expanding your global footprint or staying compliant with changing laws, this webinar will provide essential guidance to ensure your products meet local standards.

Supply Chain Traceability in the Recycling World

In this webinar, you will learn about Intertek's Recycling Supply Chain Verification Program.

The New EFSA Novel Food Guidance: What Has Changed and What Does This Mean for Future EU Applications?

This webinar will describe the changes that have been made and how best to approach new EU applications following the requirements in this updated guidance.

Webinar: Introduction to Food Safety Certification

Navigating the world of food safety certification can be overwhelming, especially with so many options available. As a food business owner, ensuring the highest standards of safety and compliance is crucial, but where do you start? Join us on September 19, 11am, for our webinar: Introduction to Food Safety Certification where we’ll break down the different certification options and guide you through the steps needed to achieve the right certification for your business.

Regulatory Requirements of China Full Version Cosmetic Product Safety Report

During this webinar, our experts will help overseas industry peers know more about China cosmetic safety assessment requirements and solutions for a full version safety report.

An Overview of the US FDA Surrogate Contamination Testing

In this webinar, discover the intricacies of the US FDA Surrogate Contamination Testing, also commonly referred to as the "Challenge Test".

Webinar Download | Review of a European Working Group Report on the Safety Assessment and Regulatory Management of Certain “Other Substances” in the EU

For further details about the pertinent regulations, proposed restrictions, and potential implications, please download our webinar.

Endocrine Disruption Assessments

This webinar will provide a general overview of endocrine disruption, regulations for EDCs in the (EU, methodology for identification of EDCs as per the ECHA/EFSA guidance, and the new REACH requirements and CLP classification criteria for EDCs in the EU.

What is Left to Know about Right to Know Legislations and The Complexities of Ensuring the Balance Between Compliance and the Expectation of Transparency as it Relates to Marketing Consumer Products

This webinar will provide information on the development and original intent of the Act, the means for a company to comply with the Act without disclosing essential business information, upcoming changes to the Acts, and how they are enforced.

Protect Your Brand | Combat Food Poisoning (English)

Food poisoning incidents not only harm your customer’s health but can also severely damage your brand's image, leading to a loss of consumer trust and satisfaction, resulting in financial losses and diminishing your market share.

Protect Your Brand | Combat Food Poisoning (Arabic)

Food poisoning incidents not only harm your customer’s health but can also severely damage your brand's image, leading to a loss of consumer trust and satisfaction, resulting in financial losses and diminishing your market share.

Webinar Download | Revisions to Health Canada's Proposes New Fees for Natural Health Products

Assuris has prepared a webinar, highlighting the new proposed NHP fees and how these differ from the original fee schedule.

On-Demand Webinar: ISO 18562 and Biocompatibility

The ISO 18562 series was developed to define testing requirements relevant to gas pathways. To better understand these requirements (and how Intertek can help you) listen to our complimentary 25-minute on-demand webinar.

Introduction to MSC & ASC Chain of Custody Certification

Marine Stewardship Council (MSC) and Aquaculture Stewardship Council (ASC) Chain of Custody certification provides assurance of the traceability of the supply chain back to a certified source which in turn drives consumer trust and opens new market opportunities for sellers of seafood, as will be discussed in our webinar on June 25, 2pm BST.

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.

Microplastic Restriction from the Commission Regulation (EU) 2023/2055

Our webinar will present the global context of the environmental issues of the microplastics and the ECHA restriction.

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.

On Demand Webinar: Medical Industry Outlook and Global Trends

Educational session on industry trends and future outlook for medical devices.

On Demand Webinar: NDcPP v2.2e versus v3.0

Webinar on updates to NDCPP IoT security standards for device compliance.

On Demand Webinar: Software As a Medical Device Compliance Requirements

Webinar on Software as a Medical Device (SaMD) and its regulatory compliance.

Cristal - Bed Bugs - Learn, Manage, Protect

Webinar on identifying, managing, and preventing bed bug infestations.

Webinar Downloads | Latest Amendments to Regulation (EU) 10/2011

Webinar on amendments to EU 10/2011 regulation for food contact materials.

On-Demand Webinar: November 2023 FDA ASCA Program Updates

FDA ASCA Program updates for medical device regulatory compliance.

Webinar Downloads | Probiotics: A Global Overview of Safety Requirements for Foods and Supplements

Global overview of safety requirements for probiotics in foods and supplements.

Webinar Downloads | California Proposition 65 Compliance for Cosmetics

Webinar on California Proposition 65 compliance for cosmetics industry.

Bitesize Webinar: UK Food Allergen Labelling

Bitesize webinar on UK food allergen labelling standards and compliance.

Bitesize Webinar: UK Nutritional Labelling

Bitesize session on UK nutritional labelling regulations for compliance.

Bitesize Webinar: UK Food Supplement Labelling

Webinar discussing UK food supplement labelling compliance requirements.

Bitesize Webinar: Acrylamide Testing for the UK and EU

Education webinar on acrylamide testing requirements for food safety in UK/EU.

Bitesize Webinar: Acrylamide Testing for the UK and EU

Webinar on acrylamide testing for food safety compliance in UK and EU markets.

Webinar: Pest Control in GFSI Schemes

Webinar on integrating pest control into GFSI-compliant food safety systems.

Webinar: Understanding validation and verification in GFSI schemes

Webinar on validation and verification in GFSI-certified food safety systems.

On-Demand Webinar: "FDA ASCA Pilot Program Updates"

Updates on FDA’s ASCA Pilot Program for medical device testing compliance.

Webinar: Overview of the changes in FSSC 22000 V6

Updates on transitioning to FSSC 22000 Version 6 for food safety certification.

Webinar Downloads | Cosmetic Product Safety Report in China

Webinar on creating safety reports for cosmetic products in China.

Webinar: Changes From Medical Device Directive (MDD) to Medical Device Regulation (MDR)

Webinar on transitioning from MDD to MDR compliance for medical devices.

Bitesize Webinar: UK Food Supplement Labelling

Webinar on labelling regulations for food supplements in the UK market.

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.

Preparing for an Unannounced Audit – How to ensure site is Audit-Ready, every day

Webinar on preparing organizations for unannounced audits to ensure compliance.

On-Demand Medical Webinar: "Evolution of Healthcare and Home Health Devices"

Webinar exploring the evolution and safety standards of home healthcare devices.

Food Defense vs Food Fraud – How to conduct Vulnerability Assessments & Mitigation Plans

Guidance on conducting vulnerability assessments to strengthen business resilience.

Bitesize On-demand webinar: UK Nutritional Labelling

Webinar covering nutritional labelling requirements in the UK for compliance.

Webinar Downloads | In Silico Methods for Toxicological Assessment

Webinar on in-silico methods for toxicological assessments in chemical products.

Webinar Downloads | New Cosmetic Ingredient Notification and Registration in China

Overview of new ingredient notification and registration in China for cosmetics.

Webinar Downloads | Safety Assessment of Pharmaceuticals Impurities (ICH Q3A, ICH Q3B and ICH M7)

Safety assessment webinar on impurities in pharmaceuticals for compliance.

Bitesize On-demand webinar: UK Food Allergen Labelling

Webinar on UK food allergen labelling regulations to ensure compliance.

Webinar: How to build a competency matrix to meet clause 7.2 requirements

Webinar on building competency matrices for meeting ISO standards.

On-Demand Webinar: "UKCA Requirements For Medical Devices"

Webinar on UKCA requirements for medical devices and compliance strategies.

New Year, New Regulations and Preparing for 2023

Overview of upcoming food safety regulations in 2023 and preparation tips.

Webinar Downloads | Cosmetics Regulation in China: Focus on Existing Ingredients

Focused webinar on compliance for existing cosmetic ingredients under China's regulations.

Webinar Downloads | Global Cosmetics Regulations: Focus on non-EU countries and overview of upcoming regulatory projects

Overview of global cosmetics regulations and upcoming regulatory projects outside the EU.

On-Demand Webinar: "Requirements for China NMPA Registration"

Webinar on NMPA registration requirements for medical devices in China.

BRCGS Food Safety Issue 9 – On-demand webinar

Overview of BRCGS Food Safety Issue 9 updates and certification.

Medical Webinar: IEC 60601-1-2 Ed. 4.1 Overview of Requirements

Overview of IEC 60601-1-2 Ed.4.1 compliance for medical devices.

Webinar Downloads | China CSAR - Raw Material Safety Data Submission: An overview of the implementation and lessons learned

Lessons learned from implementing China's CSAR for cosmetic product compliance.

On-Demand Medical Webinar: "Design It Right The First Time"

Webinar on designing medical devices correctly for compliance and efficiency.

Webinar Downloads | China CSAR: Cosmetic Raw Material Safety Data Submission

Webinar on safety data submission for cosmetic raw materials under global regulations.

Repurposing Products for Inhaled Delivery - Rapid Response Strategies

Mark Parry, Intertek Melbourn's Technical Director, will discuss rapid repurposing strategies for inhaled delivery in a webinar. He'll address challenges and considerations for effective redevelopment, emphasizing quality control to prepare drugs for clinical trials swiftly.

Webinar Downloads | South Korea: Regulatory and Scientific Requirements for Marketing of Foods and Health Functional Foods

This webinar focuses on South Korea's regulatory framework for health claims on foods and Health Functional Foods (HFFs). It covers permissible claims, authorization processes, and new opportunities under the food function claim system.

Webinar Downloads | Australia and New Zealand: The Approval Process for New Food Ingredients

The webinar will offer a comprehensive overview of the regulatory framework for new food ingredients (novel foods) in Australia and New Zealand. Topics include definition, classification, and approval processes, along with factors to consider before submitting an application.

"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.