Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
As you start to map out your global strategy, there are six key steps to follow and multiple regulations to consider. Regulatory costs and controls can vary widely from country to country, and understanding how to enter a particular market requires insight into the unique medical device regulations affecting that market. While regulatory harmonization has increased in recent years, most countries still maintain distinct medical device regulatory systems which require analysis on a market-by-market basis to fully realize compliance requirements.
Complete the form below to download the White Paper, Six-Step Guide to Global Markets: The BRIC Countries Plus Japan, authored by Bhavesh Sheth, Intertek’s Global Market Access Consultant. Explore these six steps and reveal insights into the unique medical device regulations affecting markets in China, Brazil, Russia, India, and Japan.