Common use of PERSONAL DATA OF INVESTIGATOR AND RESEARCH STAFF Clause in Contracts

PERSONAL DATA OF INVESTIGATOR AND RESEARCH STAFF. (a) Investigator consents to the collection, processing, storage and transfer of Investigator's personal data and details relating to his/her professional activities (collectively "Personal Information”) for the purposes of management and control of clinical trials, evaluation, audit, supervision, legal, regulatory, administrative, compliance and storing in an Investigator Database for current and selection of future clinical trials. Investigator consents to the transfer of such Personal Information for the aforementioned purposes, to other states/countries which do not maintain as stringent data protection standards as contemplated herein. 5.

PERSONAL DATA OF INVESTIGATOR AND RESEARCH STAFF. (a) Investigator consents to the collection, processing, storage and transfer of Investigator's ’s personal data and details relating to his/her professional activities (collectively "“Personal Information”) for the purposes of management and control of clinical trials, evaluation, audit, supervision, legal, regulatory, administrative, compliance and storing in an Investigator Database for current and selection of future clinical trials. Investigator consents to the transfer of such Personal Information for the aforementioned purposes, to other states/countries which do not maintain as stringent data protection standards as contemplated herein. 5.

PERSONAL DATA OF INVESTIGATOR AND RESEARCH STAFF. (a) Investigator consents to the collection, processing, storage and transfer of Investigator's ’s personal data and details relating to his/her professional activities (collectively "“Personal Information”) for the purposes of management and control of clinical trials, evaluation, audit, supervision, legal, regulatory, administrative, compliance and storing in an Investigator Database for current and selection of future clinical trials. Investigator consents to the transfer of such Personal Information for the aforementioned purposes, to other states/countries which do not maintain as stringent data protection standards as contemplated herein. 5.

PERSONAL DATA OF INVESTIGATOR AND RESEARCH STAFF. (a) Investigator consents to the collection, processing, storage and transfer of Investigator's personal data and details relating to his/her professional activities (collectively "Personal Information”) for the purposes of management and control of clinical trials, evaluation, audit, supervision, legal, regulatory, administrative, compliance and storing in an Investigator Database for current and selection of future clinical trials. Investigator consents to the transfer of such Personal Information for the aforementioned purposes, to other states/countries which do not maintain as stringent data protection standards as contemplated herein. 56.