Webinars by Industry: Chemicals
Chemistry Verification under PMRA's Continuous Oversight Programme
This session will provide a comprehensive guide on how to prepare and submit chemistry validations to the Pest Management Regulatory Agency (PMRA).
Demystifying Registering Microbial Fertilizers in Canada
This webinar will introduce you to the registration process, the required data elements, and the general framework that the CFIA uses for risk assessment of microbial fertilizers.
Supply Chain Traceability in the Recycling World
In this webinar, you will learn about Intertek's Recycling Supply Chain Verification Program.
PFAS: Current Legislative Landscapes and Next Steps for Manufacturers and Suppliers
During this webinar, we will discuss the current state and future of managing PFAS in your products and supply chain.
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".
Compliance and Petition Strategy of Food Contact Materials in China
Join us to gain insights into navigating FCM regulations effectively and developing successful petition strategies.
Safety Data Sheet Requirements in Asia Pacific and Emerging Markets
This webinar offers invaluable insights into navigating the complexities of SDS compliance in these dynamic markets.
Safety Data Sheet Requirements in the United States and Canada
This webinar is designed to provide actionable insights and practical advice to help you navigate these regulatory updates effectively.
Safety Data Sheet Requirements in the EU, UK and Turkey
Join us for a webinar designed to empower industry professionals with the knowledge and tools necessary to navigate complex SDS compliance regulations in the EU, UK and Turkey.
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.
Understand Your Obligations to be Compliant With Poison Centre Notification (PCN) by 01 January 2025
If you are a manufacturer, importer, downstream user and/or distributor, join this webinar to understand your obligations to be compliant with PCN according to CLP Regulation in Europe!
From Fiber to Fashion: Simplifying Sustainability with Life Cycle Assessment(LCA) and Traceability
Discover how Life Cycle Assessment (LCA) and Traceability can reshape the textile industry towards sustainability. Get actionable insights from the industry experts into how LCA and traceability can simplify sustainability efforts and drive positive change across the fashion value chain.
K-REACH Joint Registration
Join us for an explanation of the requirement for joint registration and we'll share our registration experience.
KKDIK REACH Update
Join us for an essential webinar update on the latest regulatory developments affecting non-Turkish companies seeking KKDIK REACH coverage for their Turkish customers.
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.
Bureau of Indian Standard (BIS) Certification
This webinar focuses on the BIS certification process, BIS schemes, and how we can support our clients to obtain BIS certification.
Webinar: From Screening Methods to Validated Target Methods for Extractables and Leachables Studies
Insight into method development for extractables and leachables studies
Webinar: Sustainable Approaches in Analytical Method Development
Dr. J Susanne Becker discusses sustainable analytical methods for pharmaceutical impurity determination in drug products and devices.
Per-and Polyfluoroalkyl Substances (PFAS)
Our webinar will cover how to comply with the PFAS Reporting Rule starting November 2024, including the review of the US PFAS Roadmap, and State Regulations. Our experts will also provide a review of the proposed Canadian PFAS rule.
Regulation 2022/1616/EC on Recycled Plastics for Food Contact Use: What is New Since Entry in Force in 2022?
EU Reg 2022/1616 on recycled plastics for food contact came into force on Oct 10, 2022. Stay updated on Commission and Authority guidance. Learn to submit dossiers for recycled plastic use in Europe.
Chemical Data Reporting Rule (CDR)
Our complimentary webinar will teach you how to comply with the Chemical Date Reporting Rule starting June 2024, including changes in the EPA's Central Data Exchange (CDX) required submission.
Webinar Download | Using Risk Based Compliance to Tackle Global Moving Targets
Discover the value of implementing risk-based compliance strategies in your company to navigate the evolving landscape of regulated substances, including insights on integrating them into your quality management system, amidst ongoing updates to REACH Regulation, PFAS regulations, and other emerging areas.
RDD 2022 WORKSHOP: Developing Biologics for Respiratory Delivery - Lessons and Examples from the Real World
In a workshop, the focus will be on developing effective nasal and inhaled delivery solutions for biological drug substances targeting respiratory and systemic conditions. Challenges, solutions, and real-world project examples will be discussed.
Webinar: Outsourcing Pharmaceutical Stability Storage
Tasmina Bokhari, Stability Team Leader, shares insights on selecting the right stability partner for outsourcing. Expect efficient study management, flexible storage, and regulatory compliance. Learn how stability programs are developed and controlled to meet global quality standards.
Webinar: AIM Pipeline Direct Assessment
Explore how the Direct Assessment (DA) process can assess petroleum, gas, and multi-phase pipeline integrity for regulatory compliance in our on-demand webinar. Receive informed technical guidance to maximize value and meet statutory obligations.
On Demand Webinar | Particulate Contamination Analysis in Pharmaceuticals
Particulate contamination in pharmaceuticals raised safety concerns, leading to numerous recalls. Dr. Stefan Heck will discuss identification challenges and regulatory strategies in a webinar, showcasing suitable test strategies through case studies.
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.
Translating Inhaled and Nasal Technologies for Biologic Drug Delivery
Inhaled and nasal delivery has specific advantages as a delivery platform outside of its traditional use for asthma/COPD and seasonal rhinitis/sinusitis however inhaled and nasal targets can offer advantages for the delivery of therapeutic biologics in the context of a shifting landscape for drug delivery.
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.
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.