Study Team Member Personal Sample Clauses

Study Team Member Personal. Data 6.1 Osobní údaje členů Studijního týmu 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. Jak před zahájením, tak i v průběhu provádění Studie, Zkoušející a jeho/její tým mohou být požádáni o poskytnutí svých osobních údajů. Tyto údaje spadají do rámce právních předpisů na úseku ochrany osobních údajů, konkrétně zákona č. 101/2000 Sb., o ochraně osobních údajů a o změně některých zákonů, ve znění pozdějších předpisů. For the Investigator, 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 for the following purposes: Ohledně Zkoušejícího, tyto osobní údaje mohou zahrnovat jména, kontaktní informace, pracovní zkušenosti a profesní kvalifikaci, přehled publikací, resumé, informace o absolvovaném vzdělání, a informace týkající se potenciálních střetů zájmů v souvislosti s výkonem Duální funkce, a údaje o platbách uskutečněných vůči Příjemci plateb dle této Smlouvy, a to pro následující účely: (i) the conduct of clinical trials, (i) provádění klinických hodnocení, (ii) verification by governmental or regulatory agencies, the Sponsor, Quintiles, and their agents and affiliates, (ii) ověření ze strany státních/správních nebo regulatorních úřadů, Zadavatele, Quintiles, a jejich zástupců, sesterských organizací či poboček, (iii) compliance with legal and regulatory requirements, (iii)zajištění souladu s právními a regulatorními požadavky, (iv) publication on xxx.xxxxxxxxxxxxxx.xxx and websites and databases that serve a comparable purpose; (iv)zveřejnění na stránkách xxx.xxxxxxxxxxxxxx.xxx a webových stránkách a serverech, které slouží obdobnému účelu; (v) storage in databases to facilitate the selection of investigators for future clinical trials; and (v) evidování v databázích pro účely usnadnění výběru zkoušejících pro budoucí klinická hodnocení; a (vi) anti-corruption compliance.
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Study Team Member Personal. Data 6.1 Osobní údaje členů Studijního týmu 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 Data Protection Regulation 2016/679 – GDPR and Act No. 110/2019 Coll., on Personal Data Processing, as amended. Jak před zahájením, tak i v průběhu provádění Studie, Zkoušející a jeho/její tým mohou být požádáni o poskytnutí svých osobních údajů. Tyto údaje spadají do rámce právních předpisů na úseku ochrany osobních údajů, konkrétně zákona č. 110/2019 Sb., o zpracování osobních údajů, v platném znění. For the Investigator, 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 for the following purposes: Ohledně Zkoušejícího, tyto osobní údaje mohou zahrnovat jména, kontaktní informace, pracovní zkušenosti a profesní kvalifikaci, přehled publikací, resumé, informace o absolvovaném vzdělání, a informace týkající se potenciálních střetů zájmů v souvislosti s výkonem Duální funkce, a údaje o platbách uskutečněných vůči Příjemci plateb dle této Smlouvy, a to pro následující účely: i. the conduct of clinical trials , i. provádění klinických hodnocení, ii. verification by governmental or regulatory agencies, the Sponsor, CRO, and their agents and affiliates, ii. ověření ze strany státních/správních nebo regulatorních úřadů, Zadavatele, CRO, a jejich zástupců, sesterských organizací či poboček,
Sample 1
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. 6.1 Osobní údaje členů Studijního týmu Jak před zahájením, tak i v průběhu provádění Studie, Zkoušející a jeho/její tým mohou být požádáni o poskytnutí svých osobních údajů. Tyto údaje spadají do rámce právních předpisů na úseku ochrany osobních údajů, konkrétně zákona č. 101/2000 Sb., na ochranu osobních údajů, v platném znění. For the Investigator, this personal data may include names, contact information, work experience and professional qualifications, publications, resumes, educational background and information related to potential Dual Ohledně Zkoušejícího tyto osobní údaje mohou zahrnovat jména, kontaktní informace, pracovní zkušenosti a profesní kvalifikaci, přehled publikací, resumé, informace o absolvovaném vzdělání, a informace týkající se potenciálních (i) the conduct of clinical trials, (ii) verification by governmental or regulatory agencies, the Sponsor, IQVIA, and their agents and affiliates, (iii) compliance with legal and regulatory requirements, (iv) publication on xxx.xxxxxxxxxxxxxx.xxx and websites and databases that serve a comparable purpose; (v) storage in databases to facilitate the selection of investigators for future clinical trials; and (vi) anti-corruption compliance. Names of members of Study Staff may be processed in IQVIA’ study contacts database for study-related purposes only, based on their prior consent.
Sample 1
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 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: (i) the conduct of clinical trials, (ii) verification by governmental or regulatory agencies, the Sponsor, Quintiles, and their agents and affiliates, (iii) compliance with legal and regulatory requirements, (iv) publication on xxx.xxxxxxxxxxxxxx.xxx and websites and databases that serve a comparable purpose; (v) storage in databases to facilitate the selection of investigators for future clinical trials; and (vi) anti-corruption compliance. The Investigator hereby further consents and 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 abovementioned purposes to countries other than their own country.
Sample 1

Related to Study Team Member Personal

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  • Project Manager The term “Project Manager” refers to the employee of the State who has been assigned responsibility for overseeing and managing the proper and timely implementation of the project.

  • Project Managers The JBE’s project manager is: [Insert name]. The JBE may change its project manager at any time upon notice to Contractor without need for an amendment to this Agreement. Contractor’s project manager is: [Insert name]. Subject to written approval by the JBE, Contractor may change its project manager without need for an amendment to this Agreement.

  • Contractor’s Project Manager 7.2.1 The Contractor’s Project Manager is designated in Exhibit F (Contractor’s Administration). The Contractor shall notify the County in writing of any change in the name or address of the Contractor’s Project Manager. 7.2.2 The Contractor’s Project Manager shall be responsible for the Contractor’s day-to-day activities as related to this Contract and shall meet and coordinate with County’s Project Manager and County’s Contract Project Monitor on a regular basis.

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