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., 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 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.
Study Team Member Personal Data. 1. Osobní údaje členů Studijního týmu
(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.
Study Team Member Personal Data. 1. Osobní údaje členů Studijního týmu
(i) the conduct of clinical trials, (i) provádění klinických
(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
Study Team Member Personal Data. Institution agrees that 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. For the Investigator, this personal data may include names, contact information, work experience and professional qualifications, 4.
Study Team Member Personal Data. 1. Osobní údaje členů Studijního týmu
(i) the conduct of clinical trials, (i) provádění klinických hodnocení,
(ii) verification by governmental or regulatory agencies, the Sponsor, IQVIA, and their agents and affiliates, (ii) ověření ze strany státních/správních nebo regulatorních úřadů, Zadavatele, IQVIA, 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)
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 xxx.xxxxxxxxxxxxxx.xxx 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.
Study Team Member Personal Data. 6. Osobní údaje
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. For the Investigator, this personal data may include names, contact information, work experience and professional qualifications, medical license, 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:
(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. Names of members of Study Staff may be processed in Quintiles’ study contacts database for study-related purposes only.
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, and the General Data Protection Regulation (GDPR). 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:
(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, xxxxxxxxxxxxxxxxxxxxxx.xx/, xxx.xxxx.xx/xxxxxxx/xxxxxxxxxx/ and websites and databases that serve a comparable purpose;
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 as defined in Applicable Data Protection Laws. This data falls within the scope of the law and regulations relating to the protection of personal data, in particular Act No. 110/2019 Coll., on Personal Data Processing, as amended., and as defined in Applicable Data Protection Laws and may be used by Sponsor, and its affiliates in compliance with applicable law, including as set forth below and for the length of time reasonably necessary for the purposes below. 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. Sponsor, its affiliates, or collaboration parties and agents working with the Sponsor will process such personal data of the Investigator, the Study Staff or other relevant Institution [and Research Company] personnel ("Personnel") for the following purposes: (i) the conduct of clinical trials; (ii) verification by governmental or regulatory agencies, the Sponsor, , and its agents and affiliates; (iii) compliance with legal and regulatory requirements; (iv) publication on xxx.xxxxxxxxxxxxxx.xxx, other public websites and public portals for clinical documents of EMA and other relevant agencies that inform about clinical trials and participating investigators and corresponding study results; (v) storage in databases to facilitate the selection of investigators for future clinical trials; (vi) sharing of Study reports and other Study documents with third parties for research purposes in accordance with responsible data sharing and transparency obligations; and (vii) anti-corruption compliance. 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. Zkoušející tímto dává souhlas a Zdravotnické zařízení souhlasí s tím, že poskytne součinnost při získávání jakýchkoli potřebných souhlasů Studijního personálu nebo jiného příslušného člena personálu Zdravotnického zařízení s užíváním a zpracováváním osobních údajů ze strany Zadavatele a jeho spřízněných osob nebo třetích osob spolupracujících se Zadavatelem na vývoji sloučeniny, a to pro následující účely: (i) provádění klinických h...
