2-day In-person Seminar (February 25-26, 2016)
Data Management and Statistical Issues with Clinical Trials
Clinical data management is a pretty complex process that involves collection, integration and validation of clinical trial data. It is vital for the companies and CROs conducting clinical trial to adhere to the quality standards and practices set by the regulatory agencies to stand a chance of a drug approval. Hence, it is critical that all the staff involved in clinical research are properly trained by industry experts to effectively perform data management tasks.
This two-day workshop will be conducted by an industry expert who has wealth of experience managing data in clinical trials. After attending this workshop, you can be rest assured that you will be much better equipped in managing data and statistical issues in a compliant way. The tips that the instructor will share during the course of the training program will be invaluable, regardless of where you are in your career.
Who Will Benefit:
For additional information on the workshop agenda and logistics, please call +1 877-566-4981 or +1 410-501-5777 or email: firstname.lastname@example.org