Frank has been a leader in the scientific community in promoting data disclosure and transparency in clinical research. He has published and presented extensively on the subject and been an advisor on transparency strategies to WHO, NIH, PCORI, Harvard’s Multiregional Clinical Trials Center, and other government agencies and is currently involved in 3 collaborative efforts on data sharing.   His experience has spanned protocol registration, results disclosure, and sharing of individual patient data.   He was a pivotal figure in the design and launch of what is now, one of the largest and earliest patient data sharing sites in the world.   Frank has extensive knowledge of international regulations and professional guidelines affecting data sharing.  He can help your institution develop policies and guidelines on clinical data disclosure and transparency and to develop a program to make relevant information available to patents and health care providers that will meet the expectations of regulatory agencies and professional organizations.