PERSONAL DATA OF INVESTIGATOR AND RESEARCH STAFF Sample Clauses

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.
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PERSONAL DATA OF INVESTIGATOR AND RESEARCH STAFF. (a) In order to comply with their obligations under applicable privacy and data security laws, Institution and Investigator agree to comply with the terms of the DPA in relation to Data Protection. (b) Sponsor and CRO may make available such Personal Information, as defined in the DPA, to affiliated companies of Sponsor and/or CRO, legal and regulatory agencies and authorities.
Sample 1
PERSONAL DATA OF INVESTIGATOR AND RESEARCH STAFF. DATA PROTECTION CONSENT (a) Investigator hereby consents to the collection, processing, use, storage and transfer of Investigator's personal data and details relating to his/her professional activities, such as a. contact details (business address, telephone, mobile, fax, e-mail address if applicable) b. medical qualification c. previous experience in clinical trials (indication, number of years) d. previous and current information regarding participation in Chiltern studies e. other relevant information to allow selection for appropriate clinical trials in the future (collectively “Personal Information”) by Xxxxxxxx (acting as a 5.
Sample 1
PERSONAL DATA OF INVESTIGATOR AND RESEARCH STAFF. DATA PROTECTION CONSENT (a) Investigator hereby consents to the collection, processing, use, storage and transfer of Investigator's personal data and details relating to his/her professional activities, such as a. contact details (business address, telephone, mobile, fax, e-mail address if applicable) b. medical qualification c. previous experience in clinical trials (indication, number of years) d. previous and current information regarding participation in Xxxxxxxx studies 5.
Sample 1
PERSONAL DATA OF INVESTIGATOR AND RESEARCH STAFF. (a) In order to comply with their obligations under applicable privacy and data security laws, Institution and (i) provést nezávislé lékařské posouzení, zda jednotlivé Subjekty hodnocení splňují požadavky Protokolu; (ii) informovat společnost Covance a Zadavatele o jakýchkoliv případných odchylkách od Protokolu nebo jeho nedodržování; (iii) neprodleně odpovídat na všechny dotazy společnosti Covance nebo Zadavatele na jakékoli záležitosti týkající se Studie; (iv) neprodleně společnost Covance informovat o jakýchkoli významných změnách, které se vyskytnou kdykoli v průběhu Studie a které mohou mít vliv na schopnost Zkoušejícího nebo Zdravotnického zařízení provést Studii, zejména o změnách pracovníků účastnících se Studie (d) Povinnosti Zdravotnického zařízení (i) Zdravotnické zařízení se zavazuje, že jeho Výzkumný personál vynaloží maximální úsilí s cílem přesně a efektivně provádět práce požadované podle této Smlouvy, přičemž se zejména jedná o položky (i) až (iv) uvedené v bodě 3 písm. b) výše.
Sample 1
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 kroky za účelem zajištění přesnosti a úplnosti informování Zadavatele, společnosti Xxxxxxxx a Etické komise/institucionální hodnotící komise o jakýchkoliv odchylkách od Protokolu nebo jeho nedodržování;
Sample 1
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. (b) Xxxxxxxx may make available such Personal Information to affiliated companies of Sponsor and/or Xxxxxxxx, legal and regulatory agencies and authorities. 5.
Sample 1
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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. (b) Chiltern may make available such Personal Information to affiliated companies of Sponsor and/or Chiltern, legal and regulatory agencies and authorities. se studie; (iv) neprodlené oznámení jakýchkoliv významných změn, které se vyskytnou kdykoliv během studie, jež mohou nepříznivě ovlivnit schopnost zkoušejícího nebo zdravotnického zařízení provádět studii, zejména změny personálu podílejícího se na studii, Chiltern; (v) řádné dokumentování postupů ve studii podle požadavků protokolu nebo pokynů.
Sample 1

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