Study Staff Personal Data Sample Clauses

Study Staff Personal Data. 6.1 Osobní údaje Studijního personálu 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 the applicable data protection legislation enacted under the same or equivalent/similar national legislation (collectively "Data Protection Legislation"). 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 may be used by IQVIA, GSK, and their affiliates in compliance with Data Protection Legislation, including as set forth below and for the length of time reasonably necessary for the purposes below. Jak před zahájením, tak i v průběhu provádění Studie, Zkoušející a jeho/její tým mohou být požádáni o poskytnutí „Osobních údajů“, jak jsou tyto definovány příslušnými právními předpisy na ochranu osobních údajů, vydanými na základě shodné či ekvivalentní/obdobné národní legislativy (společně dále jen „Předpisy na ochranu 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, a mohou být používány společností IQVIA, GSK a jejich přidruženými subjekty v souladu s Předpisy na ochranu osobních údajů, včetně toho, jak je uvedeno níže, a to po dobu přiměřeně potřebnou k níže uvedeným účelům. GSK, IQVIA, and Institution will cooperate with each other to take the necessary measures to ensure adherence to Data Protection Legislation. Institution is responsible for supplying the Investigator and Study Staff with sufficient information regarding the collection of, handling, and use of their Personal Data. GSK, IQVIA a Poskytovatel budou vzájemně spolupracovat na potřebných opatřeních k zajištění dodržování Předpisů na ochranu osobních údajů. Poskytovatel odpovídá za to, že Zkoušejícímu a Studijnímu personálu poskytne dostatečné informace ohledně shromažďování jejich Osobních údajů, nakládání s nimi a jejich použití. This Personal Data may include names, contact information, work experience and professional qualifications, publications, resumes, educational background and information related to financial disclosures or other potential conflict of interest, and Tyto Osobní údaje mohou zahrnovat jména, kontaktní informace, pracovní zkušenosti a profesní kvalifikaci, přehled publikací, resumé, informace o absolvovaném vzdělání, a informace t...
Sample 1Sample 2See All (4)
AutoNDA by SimpleDocs
Study Staff Personal Data. 6.1 Osobní údaje Studijního personálu 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 the applicable data protection legislation enacted under the same or equivalent/similar national legislation (collectively “Data Protection Legislation”). 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, and Regulation of the European Parliament and the Council (EU) 2016/679 from 7 April 2016 on Personal Data Protection („GDPR“) and may be used by IQVIA, GSK, and their affiliates in compliance with Data Protection Legislation, including as set forth below and for the length of time reasonably necessary for the purposes below. For the Investigator and Study Team members, this Personal Data may include names, contact information, work experience and professional qualifications, publications, resumes, educational background and information related to financial disclosures or other potential conflict of interest, and payments made to Payee(s) under this Agreement for the following purposes: Jak před zahájením, tak i v průběhu provádění Studie, Zkoušející a jeho/její tým mohou být požádáni o poskytnutí „Osobních údajů“ definovaných v příslušné legislativě xx xxxxxxx xxxxxxxx xxxxx xxxxxxx xxxx transpozicí do národního práva nebo v ekvivalentní/podobné národní legislativě (společně „Legislativa na ochranu 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, a Nařízení Evropského parlamentu a Rady (EU) 2016/679 ze dne 27. dubna 2016 o ochraně osobních údajů („GDPR“) a mohou být používány společností IQVIA, GSK a jejich přidruženými subjekty v souladu s Legislativou na ochranu osobních údajů, jak je uvedeno níže, a po přiměřenou dobu nezbytnou k níže uvedeným účelům. Ohledně Zkoušejícího a členů Studijního týmu tyto osobní údaje mohou zahrnovat jména, kontaktní informace, pracovní zkušenosti a profesní kvalifikaci, přehled publikací, resumé, informace o absolvovaném vzdělání, a informace týkající se finančních vztahů nebo dalších potenciálních střetů zájmů a údaje o platbách uskutečněných vůči Příjemci plateb dle této Smlouvy, a to pro následující účely:
Sample 1
Study Staff Personal Data. Both prior to and during the course of the Study, the Investigator and Study Staff may be called upon to provide personal data. Site shall collect, handle, process, store and use all personal data of Investigator and Study Staff in accordance with the Applicable Law.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, 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. The Institution acknowledges that the Investigator consents to Sponsor’s, its designees’, and Quintiles’ collection, processing, storage, and use of his or her personal data for the purposes 5.6 Přetrvávající platnost Tento článek 5 „Práva na zveřejnění” zůstane v platnosti i v případě ukončení platnosti či po vypršení platnosti této Smlouvy. 6.
Sample 1
Study Staff Personal Data. 6.1 Osobní údaje Studijního personálu 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 the applicable data protection legislation enacted under the same or equivalent/similar national legislation (collectively “Data Protection Legislation”). This data falls within the scope of the law and regulations relating to the protection of Personal Data, in particular General Data Protection Regulation (EU) 2016/679 (“GDPR”) and Act No. 110/2019 Coll., on Personal Data Processing, and may be used by IQVIA, GSK, and their affiliates in compliance with Data Protection Legislation, including as set forth below and for the length of time reasonably necessary Jak před zahájením, tak i v průběhu provádění Studie, Zkoušející a jeho/její tým mohou být požádáni o poskytnutí „Osobních údajů“ definovaných v příslušné legislativě na ochranu osobních údajů přijaté její transpozicí do národního práva nebo v ekvivalentní/podobné národní legislativě (společně „Legislativa na ochranu osobních údajů“). Tyto údaje spadají do rámce právních předpisů na úseku ochrany osobních údajů, zejména Obecného nařízení (EU) 2016/679 o ochraně osobních údajů („GDPR“) a zákona č. 110/2019 Sb., o zpracování osobních údajů, v platném znění, a mohou být používány společností IQVIA, GSK a jejich přidruženými subjekty v souladu s Legislativou na ochranu for the purposes below. osobních údajů, jak je uvedeno níže, a po přiměřenou dobu nezbytnou k níže uvedeným účelům. GSK, IQVIA, and Institution will cooperate with each other to take the necessary measures to ensure adherence to Data Protection Legislation. Sponsor is responsible for supplying the Investigator and Study Staff with sufficient information regarding the collection of, handling, and use of their Personal Data. This Personal Data may include names, contact information, work experience and professional qualifications, publications, resumes, educational background and information related to financial disclosures or other potential conflict of interest, and payments made to Payee(s) under this Agreement for the following purposes:
Sample 1
Study Staff Personal Data. Both prior to and during the course of the Study, the Investigator and Study Staff may be called upon to provide personal data. Site shall collect, handle, process, store and use all personal data of Investigator and Study Staff in accordance with the Applicable Law.This data falls within the scope of the law and rozsahu v této souvislosti, jakékoli Nepublikované údaje jakékoli třetí straně ani nezveřejní jakákoli Studijní data či údaje jakékoli třetí straně, a to v rozsahu xxxxxx, xxxxx x xxxxx xxxxx xxx zpřístupněny v jakékoli publikaci, prezentaci či jiném odhalení na základě části 5.1 nebo 5.2. 5.4 K ontakty s médii Zdravotnické zařízení nebude a zajistí, že zaměstnanci Zdravotnického zařízení nebudou poskytovat jakékoli rozhovory či jiné formy kontaktů s médii, zejména s vydavatelstvími novin, provozovateli radiového vysílání, provozovateli televizního vysílání a společnostmi působícími na internetu, a to v souvislosti se Studií, Hodnoceným léčivem, Objevy nebo Studijními daty a údaji, bez předchozího písemného svolení Zadavatele. Toto ustanovení nebrání možnosti publikovat či prezentovat Studijní data a údaje v souladu s tímto Článkem 5. 5.5 Použití názvu či jména, registrace a oznamování Žádná Strana této Smlouvy není oprávněna použít jména či názvu jiné Strany a názvu Zadavatele, a to v souvislosti s jakoukoli reklamní činností, k publikačním či marketingovým účelům bez předchozího písemného svolení, s výjimkou případů, kdy Zadavatel a Quintiles budou oprávněni použít názvu Zdravotnického zařízení v souvislosti s publikacemi týkajícími se Studie a v rámci komunikace, včetně xxxxxxxx xxxxxxx xxxxxxxxxx xxxxxxxxx hodnocením a pro účely newsletterů vydávaných v souvislosti se Studií. Zadavatel bude Studii registrovat v souladu s příslušnými právními předpisy a bude oznamovat výsledky Studie veřejně ve lhůtě a v rozsahu uloženém příslušnými právními předpisy. 5.6 Přetrvávající platnost Tento článek 5 „Práva na zveřejnění” zůstane v platnosti i v případě ukončení platnosti či po vypršení platnosti této Smlouvy. 6.
Sample 1
Study Staff Personal Data. Both prior to and during the course of the Study, the Site and its Study Staff may be called upon to provide IQVIA and the Sponsor with 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 Studijního personálu Jak před zahájením, tak i v průběhu provádění Studie mohou být Místo provádění klinického hodnocení a jeho Studijní personál požádáni o poskytnutí svých osobních údajů společnosti IQVIA a Zadavateli. 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. This Personal Data may include Investigator or Study Staff 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 (as defined in Tyto Osobní údaje mohou zahrnovat jména Zkoušejícího nebo Studijního personálu, 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
Sample 1

Related to Study Staff Personal Data

  • Processing of Personal Data (a) SORACOM collects and processes personal data about the Subscriber, including name, e-mail, IP-address as well as data on data uses and billing data in order to provide SORACOM’s service and other purposes such as billing.

  • Your Personal Data 17.1. PFS is a registered Data Controller with the Information Commissioners Office in the UK under registration number Z1821175 xxxxx://xxx.xxx.xx/ESDWebPages/Entry/Z1821175

  • Transfer of Personal Information Supplier warrants to DXC that Personal Information provided to Supplier or obtained by Supplier under this Agreement on behalf of DXC (including any SOW) shall not be transferred across national boundaries unless authorized by law or specified within this Agreement or the applicable SOW as authorized for transfer across national boundaries. Supplier agrees that any such transfer will only be made in compliance with applicable Data Privacy Laws. If there is a conflict between this Section ‘Data Protection and Privacy’ and the other provisions of this Agreement, the requirements of this Section shall take precedence.

  • Transfer of Personal Data The Participant authorizes, agrees and unambiguously consents to the transmission by the Company (or any Subsidiary) of any personal data information related to the Option awarded under this Agreement for legitimate business purposes (including, without limitation, the administration of the Plan). This authorization and consent is freely given by the Participant.

  • Types of Personal Data Contact Information, the extent of which is determined and controlled by the Customer in its sole discretion, and other Personal Data such as navigational data (including website usage information), email data, system usage data, application integration data, and other electronic data submitted, stored, sent, or received by end users via the Subscription Service.

  • Personal Data Registry Operator shall (i) notify each ICANN-­‐accredited registrar that is a party to the registry-­‐registrar agreement for the TLD of the purposes for which data about any identified or identifiable natural person (“Personal Data”) submitted to Registry Operator by such registrar is collected and used under this Agreement or otherwise and the intended recipients (or categories of recipients) of such Personal Data, and (ii) require such registrar to obtain the consent of each registrant in the TLD for such collection and use of Personal Data. Registry Operator shall take reasonable steps to protect Personal Data collected from such registrar from loss, misuse, unauthorized disclosure, alteration or destruction. Registry Operator shall not use or authorize the use of Personal Data in a way that is incompatible with the notice provided to registrars.

  • Transfers of Personal Data Oracle may store or transfer Your Content on a global basis as necessary for the Purpose(s). Oracle and its affiliates may perform certain aspects of the Services (e.g., administration, maintenance, support, disaster recovery, data processing, etc.) from locations and through subcontractors, worldwide. Data transfers are made subject to the terms of the EU Standard Contractual Clauses for Controllers (“Clauses”) if: (a) You (or Your data partner) share, use, or process Personal Data under this Agreement; and (b) such data transfer is: (i) subject to any restrictions or requirements under Directive 95/46/EC or Regulation (EU) 2016/679 repealing Directive 95/46/EC (General Data Protection Regulation); and (ii) made to countries, jurisdictions or recipients outside the EEA or Switzerland not recognized by the European Commission as ensuring an adequate level of protection pursuant to Directive 95/46/EC or General Data Protection Regulation. You and Oracle agree that incorporation of the Clauses into this Agreement acts as a legally-binding execution of the Clauses as entered into between Oracle (acting in its own name and in the name and on behalf of the Oracle affiliates) and You (acting in Your own name and in the name and on behalf of Your affiliates).

  • Use of Personal Data By executing this Stock Agreement, Participant acknowledges and agrees to the collection, use, processing and transfer of certain personal data, including his or her name, salary, nationality, job title, position and details of all past Awards and current Awards outstanding under the Plan (“Data”), for the purpose of managing and administering the Plan. The Participant is not obliged to consent to such collection, use, processing and transfer of personal data, but a refusal to provide such consent may affect his or her ability to participate in the Plan. The Company, or its Subsidiaries, may transfer Data among themselves or to third parties as necessary for the purpose of implementation, administration and management of the Plan. These various recipients of Data may be located elsewhere throughout the world. The Participant authorizes these various recipients of Data to receive, possess, use, retain and transfer the Data, in electronic or other form, for the purposes of implementing, administering and managing the Plan. The Participant may, at any time, review Data with respect to the Participant and require any necessary amendments to such Data. The Participant may withdraw his or her consent to use Data herein by notifying the Company in writing; however, the Participant understands that by withdrawing his or her consent to use Data, the Participant may affect his or her ability to participate in the Plan.

  • Handling Sensitive Personal Information and Breach Notification A. As part of its contract with HHSC Contractor may receive or create sensitive personal information, as section 521.002 of the Business and Commerce Code defines that phrase. Contractor must use appropriate safeguards to protect this sensitive personal information. These safeguards must include maintaining the sensitive personal information in a form that is unusable, unreadable, or indecipherable to unauthorized persons. Contractor may consult the “Guidance to Render Unsecured Protected Health Information Unusable, Unreadable, or Indecipherable to Unauthorized Individuals” issued by the U.S. Department of Health and Human Services to determine ways to meet this standard.

  • Authorization to Release and Transfer Necessary Personal Information The Grantee hereby explicitly and unambiguously consents to the collection, use and transfer, in electronic or other form, of the Grantee’s personal data by and among, as applicable, the Company and its Subsidiaries for the exclusive purpose of implementing, administering and managing the Grantee’s participation in the Plan. The Grantee understands that the Company may hold certain personal information about the Grantee, including, but not limited to, the Grantee’s name, home address and telephone number, date of birth, social security number (or any other social or national identification number), salary, nationality, job title, number of Award Units and/or shares of Common Stock held and the details of all Award Units or any other entitlement to shares of Common Stock awarded, cancelled, vested, unvested or outstanding for the purpose of implementing, administering and managing the Grantee’s participation in the Plan (the “Data”). The Grantee understands that the Data may be transferred to the Company or to any third parties assisting in the implementation, administration and management of the Plan, that these recipients may be located in the Grantee’s country or elsewhere, and that any recipient’s country (e.g., the United States) may have different data privacy laws and protections than the Grantee’s country. The Grantee understands that he or she may request a list with the names and addresses of any potential recipients of the Data by contacting his or her local human resources representative or the Company’s stock plan administrator. The Grantee authorizes the recipients to receive, possess, use, retain and transfer the Data, in electronic or other form, for the sole purpose of implementing, administering and managing the Grantee’s participation in the Plan, including any requisite transfer of such Data to a broker or other third party assisting with the administration of Award Units under the Plan or with whom shares of Common Stock acquired pursuant to the vesting of the Award Units or cash from the sale of such shares may be deposited. Furthermore, the Grantee acknowledges and understands that the transfer of the Data to the Company or to any third parties is necessary for the Grantee’s participation in the Plan. The Grantee understands that the Grantee may, at any time, view the Data, request additional information about the storage and processing of the Data, require any necessary amendments to the Data or refuse or withdraw the consents herein by contacting the Grantee’s local human resources representative or the Company’s stock plan administrator in writing. The Grantee further acknowledges that withdrawal of consent may affect his or her ability to vest in or realize benefits from the Award Units, and the Grantee’s ability to participate in the Plan. For more information on the consequences of refusal to consent or withdrawal of consent, the Grantee understands that he or she may contact his or her local human resources representative or the Company’s stock plan administrator.

Time is Money Join Law Insider Premium to draft better contracts faster.