Intertek to Exhibit at DIA 2016
08 Jun 2016
Mississauga, Ontario - Intertek, a leading Total Quality Assurance provider to industries worldwide, will be exhibiting at Booth #1637 at the upcoming DIA (Drug and Information Association) 52nd Annual Meeting from June 26-30, 2016, in Philadelphia, PA, USA.
The Intertek regulatory consulting and laboratory services teams can help guide clients through the complex hurdles of medical product development. Understanding the challenges related to product classification can be very complex. The legal framework in each country will impact whether your product is a cosmetic, a medical device or a drug. Product classification has become very complex as regulatory guidelines vary across different regions. Intertek’s regulatory experts can assist clients with product classification, based on ingredients and intended claims. Additionally, they can help clients meet the regulatory requirements in each desired country for marketing.
Intertek’s laboratory services team conducts bioanalytical, analytical and formulation development services which are aligned with helping clients progress along the development pipeline, and reduce the costs and uncertainties associated with complex development programs.
To set-up a meeting during the show, please contact pharma.sci-reg@intertek.com.
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/scientific-regulatory-consultancy/
About Intertek
Intertek is a leading Total Quality Assurance provider to industries worldwide. Our network of more than 1,000 laboratories and offices and over 40,000 people in more than 100 countries, delivers innovative and bespoke Assurance, Testing, Inspection and Certification solutions for our customers’ operations and supply chains.
Bringing quality and safety to life
About Intertek Pharmaceutical Services
Intertek’s consultants and experts provide assistance at all stages of product development to clients in the pharmaceutical, biotechnology and medical device fields. With diverse and in-depth experience, our team of scientists and regulatory affairs specialists provide expert advice and services related to nonclinical safety testing, manufacturing, clinical trial design, submission preparation, regulatory agency interactions, and more. Supported by our offices in the United States, Canada, Europe and Asia, we work with clients worldwide to develop strategies to effectively meet their urgent and long-term global product development needs. https://www.intertek.com/pharmaceutical/consulting/
For Media Inquiries:
Heather Wilson
Senior Conference Administrator
Intertek Scientific & Regulatory Consultancy
Tel: +1 905 542 2900
Email: heather.wilson@intertek.com
For Market Inquiries:
Anna Metcalfe
Vice President, Regulatory Affairs
Intertek Scientific & Regulatory Consultancy
Tel: +1 905 542 2900
Email: anna.metcalfe@intertek.com