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.
Intertek, a leading Total Quality Assurance provider to industries worldwide, will be exhibiting at Booth #613 at DIA's (Drug and Information Association) 53rd Annual Meeting taking place in Chicago, Illinois, from June 18th-22nd, 2017.
DIA 2017 is a highly anticipated event as it is the largest, longest-run meeting in the life sciences industry. This year's theme will focus on "Driving Insights to Action" and attendees will benefit from global insights to improve health through the development of technologies and lifesaving medicines. DIA 2017 will attract more than 7,000 global health care professionals in the pharmaceuticals, biotechnology, and medical device industries from more than 51 countries worldwide. Attendees are able to choose form over 160 sessions and meet with more than 450 exhibiting companies.
DIA 2017 is the Ideal platform for stakeholders wishing to gain additional knowledge in the field of new therapies and contribute to discussions on health and well-being. This must-attend event will provide participants an opportunity to exchange knowledgeable information and insights beyond boundaries to advance innovation in health care product development and life cycle management globally.
Intertek Health, Environmental & Regulatory Services (HERS), along with our laboratory services teams can help guide clients through the complex hurdles for pharmaceutical and healthcare product development and regulatory requirements. For example, understanding the challenges related to product classification can be very complex as the legal framework varies across different regions which impacts the classification of a product. Intertek’s regulatory experts can assist clients with product classification, based on product design, formulations, intended claims, etc. Additionally, they can help clients meet the regulatory requirements in each desired country for marketing. To set-up a meeting during the show, please contact email@example.com or visit us at Booth #613.
To learn more about the regulatory and scientific consultancy services offered by our experts and within the larger Intertek organization visit: http://www.intertek.com/pharmaceutical/
Total Quality. Assured.
Intertek is a leading Total Quality Assurance provider to industries worldwide. Our network of more than 1,000 laboratories and offices and over 42,000 people in more than 100 countries, delivers innovative and bespoke Assurance, Testing, Inspection and Certification solutions for our customers' operations and supply chains. Intertek Total Quality Assurance expertise, delivered consistently with precision, pace and passion, enabling our customers to power ahead safely.
Global Marketing Manager
T: +1 905 542 2900
Vice President, Regulatory Affairs
T: +1 905 542 2900