Product Recalls Returns to Indy! For nearly ten years, CBI has delivered key updates and best practices for successful execution of drug, device and diagnostic recalls corrections. Join us this year to hear industry case studies and effectively prepare for recall/field correction situations. Register today or click here to learn more!
Join West for a free, full-day seminar discussing development considerations and quality drivers for injectable container closure and delivery systems. The seminar includes educational materials and a tour of our state-of-the-art Analytical Laboratory and R&D Center. Register: http://bit.ly/hCqEQi
A one-day class delivering an overview of the discovery, development, and regulatory processes for bringing a new drug to market. Participants will learn about the business and scientific decisions involved in moving a product forward from basic research into preclinical and clinical trials. Register Now!
Join 7,000+ life sciences professionals involved in the discovery, development, and life cycle management of medical products all with a common goal to foster innovation that will lead to the development of safe and effective medical products and therapies to patients at the DIA 2013 49th Annual Meeting: Advancing Therapeutic Innovation and Regulatory Science. This year’s meeting will offer 250+ sessions over 22 tracks on the hottest topics in the industry. Register Today!
The largest event for life science marketers returns to the west coast! Join 300+ attendees for the latest in mobile, web, and social media strategies. Featuring 18 new case studies, pharma only networking events, and an entire day dedicated to Mobile. Click here for more information.
BioBasics is a two-day course for the non-scientist which highlights science and technology concepts that are the basis of the biotechnology industry. The course is for participants that require a working knowledge of fundamental terms and applications. Register today.
A one-day class delivering an overview of the discovery, development, and regulatory processes for bringing a new drug to market. Participants will learn about the business and scientific decisions involved in moving a product forward from basic research into preclinical and clinical trials. Learn More.