This course builds upon the clinical regulatory foundation built in IRA001. It provides you with an understanding of the trends in pharmaceutical industry, with regards to policy making and product development. The topics also in include regulatory strategies in developing a product and post approval management of the product. You will have a good understanding of regulatory strategies in developing a product and post approval management of the product, along with PMS and related regulations. 25 Watline Ave, Suite #201, Mississauga, ON, L4Z 2Z1IRA004 – Professional Regulatory Affairs
Duration : 1 Day
Time : 9 AM – 5 PM
Who should attend?