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
Home Healthcare Medical Devices | FAQ
The home healthcare market offers significant opportunities but also complex compliance and safety challenges for manufacturers. Download our new FAQ sheet "Safety and Performance Compliance For Home Healthcare Medical Devices" to learn more.
Six Compliance-Related Questions About Connected Home Healthcare Devices | White Paper
The home healthcare market is growing rapidly and device manufacturers are developing new innovations to improve patient care. Launching connected devices in the home. Download our white paper that addresses six compliance questions about connected devices in the home.
UL 60335-2-40 Latest Requirements for Certification
Big changes are here for HVAC/R manufacturers and professionals. As of January 1, 2025, UL 1995 is officially replaced by UL 60335-2-40. Are you fully prepared? Download our free white paper for answers to the most pressing questions.
CSDDD & CSRD – Step-by-Step Guide to Align Compliance Efforts for the EU’s Directives
EU Member States and Parliament approved the ‘Stop-the-clock' directive this week, which delays reporting requirements under CSRD and CSDDD as part of the proposed Omnibus simplification package. Despite this announcement many companies still need to continue working towards CSRD and CSDDD compliance.
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.
The evolution of the home healthcare market
Explore key considerations in meeting IEC 60601-1-11 requirements for safety and performance in home healthcare devices.
The evolution of the home healthcare market
Discover the latest updates on IEC 60601-1-11, focusing on home healthcare medical electrical equipment.