Study Team Member Personal Data. Both prior to and during the course of the Study, the Investigator and his/her teams may be called upon to provide personal data. This data falls within the scope of the law and regulations relating to the protection of personal data, in particular Act No. 101/2000 Coll., on Personal Data Protection, as amended. This personal data may include names, contact information, work experience and professional qualifications, publications, resumes, educational background and information related to potential Dual Capacity conflict of interest, and payments made to Payee(s) under this Agreement. The Investigator hereby consents and the Institution agrees to assist in obtaining any necessary consent from the Study Staff or other relevant Institution personnel for the use and processing of their personal data by the Sponsor and its affiliates or third parties working with the Sponsor on the development of the compound for the following purposes: the conduct of clinical trials, verification by governmental or regulatory agencies, the Sponsor, Quintiles, and their agents and affiliates, compliance with legal and regulatory requirements, publication on ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ and websites and databases that serve a comparable purpose; storage in databases to facilitate the selection of investigators for future clinical trials; and anti-corruption compliance. The Investigator hereby further consents and the Institution agrees to assist in obtaining any necessary consents from the Study Staff or other relevant Institution personnel to the transfer of such data for the above mentioned purposes to countries other than their own country.
Appears in 1 contract
Sources: Clinical Trial Agreement
Study Team Member Personal Data. Both prior to and during the course of the Study, the Investigator and his/her teams may be called upon to provide personal data. This data falls within the scope of the law and regulations relating to the protection of personal data, in particular Act No. 101/2000 Coll., on Personal Data Protection, as amended. This personal data may include names, contact information, work experience and professional qualifications, publications, resumes, educational background and information related to potential Dual Capacity conflict of interest, and payments made to Payee(s) under this Agreement. The Investigator hereby consents and the Institution Provider agrees to assist in obtaining any necessary consent consents from the Study Staff or other relevant Institution Provider personnel for the use and processing of their personal data by the Sponsor and its affiliates or third parties working with the Sponsor on the development of the compound for the following purposes: the conduct of clinical trials, verification by governmental or regulatory agencies, the Sponsor, Quintiles, and their agents and affiliates, compliance with legal and regulatory requirements, publication on ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ and websites and databases that serve a comparable purpose; storage in databases to facilitate the selection of investigators for future clinical trials; and anti-corruption compliance. The Investigator hereby further consents and the Institution Provider agrees to assist in obtaining any necessary consents from the Study Staff or other relevant Institution Provider personnel to the transfer of such data for the above mentioned purposes to countries other than their own country.
Appears in 1 contract
Sources: Clinical Trial Agreement