US · Masters
M S Drug Regulatory Affairs
Program information
Program overview
With pressure to contain the cost and time it takes to create new products and bring them to market professionals with expertise in regulatory affairs are highly sought after by pharmaceutical companies and medical device manufacturers as well as by hospitals health maintenance organizations HMOs and a range of other health care oriented organizations as well The expertise of a DRA professional may be used in areas such as clinical trials manufacturing compliance patenting sales and marketing IT finance and scientific writing
Duration: 12
Fees and entry information
No fee information is listed.
Intakes and application timing
No current intake dates are published for this program.
This program page summarizes currently published records. A match or listing is not an eligibility assessment. Universities determine entry, offer and scholarship decisions.