#21: The IDMP Challenge: Points to Consider for Pharmacovigilance Departments
- Director, R&D
- HighPoint, United States
Mr. Vanggaard is a strong team player and a results-driven senior Life Sciences R&D consultant with 9+ years of experience within Clinical Development and Regulatory Affairs implementing Clinical Data Warehouses, Meta Data Repositories, Clinical Trial Management Systems, Electronic Trial Master Files and helping more than 5 clients prepare for IDMP implementation. In addition, Mr. Vanggaard is working closely together with the HighPoint Solutions Master Data Management Practice Lead on developing an MDM-based IDMP accelerator leveraging one of the leading platforms on the market and capable of handling unstructured data from documents.