White Papers

Through its in-depth interactions with global clients in a diverse set of industries, Intertek is able to capture real-world experience and best practices in an ever-expanding White Paper library.

Most Recent White Papers

IEC 60601-2-10 Edition 2.2 (2023) | FAQ Paper

To ensure a smooth transition from IEC 60601-2-10 Edition 2.1 to Edition 2.2, Intertek's medical device experts have created a comprehensive Q&A document clarifying these essential updates and regulatory implications. Download your copy and confidently navigate this important regulatory update.

AI-Enabled Medical Device Development | FAQ Paper

Intertek's new guide, "Key Questions for AI-Enabled Medical Device Development," addresses essential factors of Artificial Intelligence (AI) and Machine Learning (ML) for Medical Devices including: clinical problem definition, representative test data, transparency of AI decisions, cybersecurity, and model validation.

Whitepaper: Adopting AI-Driven Solutions

In a rapidly evolving market, leveraging AI is key to maintaining a competitive edge. Our whitepaper provides actionable insights into how AI can revolutionise your workflows, from automating routine tasks to optimising supply chains and enhancing decision-making processes. Key Outcomes: - Gain a thorough understanding of AI’s potential and its practical applications. - Learn how to address and mitigate security and compliance challenges effectively. Download the whitepaper now to start harnessing AI for greater productivity and security in your organisation.

EU General Product Safety Regulation (GPSR): A Comprehensive Guide

Explore our comprehensive whitepaper on the General Product Safety Regulation (GPSR), designed for those unfamiliar with this crucial EU regulation. Learn about compliance requirements, key provisions, and some common questions to ensure consumer safety in the evolving regulatory landscape.

White Paper: Ensuring Compliance with Safety Data Sheets

This white paper provides a comprehensive overview of SDS regulatory requirements in the US and Canada.

White paper - Analytical assurance of concentration and quality of hyaluronic acid-based products

Learn how to accurately quantify hyaluronic acid in medical and cosmetic products with expert insights from LaCoMeD’s Allan Desrumaux. Discover the best extraction, purification, and concentration methods.

Securing the Hybrid Workforce

Download our whitepaper for insights on effectively securing your hybrid work environment and protecting sensitive data.

Adopting AI-Driven Solutions

Discover how AI can transform your workflows and boost productivity with our whitepaper.

White Paper - Analysis of Metals in Cosmetic Products

Quantifying trace metals in cosmetics is vital due to EU regulations. Effective lab testing ensures safe products by guiding raw material selection, reducing contamination risk, and guaranteeing consumer safety.

White Paper - Analytical study of a nanomaterials in a raw material

Nanomaterials have unique properties but pose health and environmental risks. Evolving regulations ensure safe use, especially in cosmetics, biocides, and food. Learn more from expert Khalil Abdelkebir.

White Paper: European Union Carbon Border Adjustment Mechanism (CBAM)

EU Regulation 2023/956 introduces the Carbon Border Adjustment Mechanism, mandating importers to report emissions of goods into the EU from Oct 1, 2023.

Whitepaper: Digital Product Passports for Sustainability, Traceability and Transparency in Apparel and Toys Industries

Sustainability, Traceability, and Transparency in apparel and toys are crucial. Our white paper explores regulatory landscapes, digital passports, and solutions.

LCV 2023 - Access our white papers and webinars

Explore the latest insights and compliance solutions for lithium-ion battery testing and certification in electric vehicles.

White Paper | From Extractables to Leachables: Problem Solving for Complicated Formulations and Container Closure Systems

Learn about critical problem-solving approaches for managing extractables and leachables in pharmaceutical products.