Personal Data Protection and Privacy. The Parties recognize a common goal of securing all personal data and holding such information in confidence and protecting it from unauthorized disclosure. The Parties represent and warrant that they will comply with the provisions of Applicable Law relating to the confidentiality, privacy and security of such personal data. In addition, the Institution and Principal Investigator shall comply with the following provisions: 10. Ochrana osobních údajů a soukromí. Strany jsou si vědomy společného cíle zabezpečení všech osobních údajů a zachování jejich důvěrnosti a ochrany před neoprávněným zveřejněním. Strany prohlašují a zaručují, že budou dodržovat všechna ustanovení platných zákonů upravujících důvěrnost, ochranu soukromí a zabezpečení těchto osobních údajů. Dále budou zdravotnické zařízení a hlavní zkoušející dodržovat následující ujednání:
Personal Data Protection and Privacy. The Parties recognize a common goal of securing all personal data and holding such information in confidence and protecting it from unauthorized disclosure. The Parties represent and warrant that they will comply with the provisions of Applicable Law relating to the confidentiality, privacy and security of such personal data. In addition, the Provider and Principal Investigator shall comply with the following provisions: 10.1.
Personal Data Protection and Privacy. A. The parties agree that (i) both ADARA and Customer are Data Controllers in respect of all Personal Data processed in relation to Services. Both parties shall comply with all Data Protection Laws that apply to it in respect of the performance of its obligations under this Agreement. The parties agree that they are not joint controllers of any data.
Personal Data Protection and Privacy. The parties undertake to conduct the Trial in accordance with Regulation (EU) 2016/679 of the European Parliament and of the Council of 27 April 2016 on the protection of natural persons with regard to the processing of personal data and on the free movement of such data, and repealing Directive 95/46/EC and Act No. 18/2018 Coll. on the Protection of Personal Data, as amended. 8.1.
Personal Data Protection and Privacy. The Parties recognize a common goal of securing all personal data and holding such information in confidence and protecting it from unauthorized disclosure. Sponsor shall be an independent data controller with respect to its processing of personal data contained in the Study related personal data reported by Principal Investigator to Sponsor or CRO. The CRO is acting as a data processor solely on behalf of the Sponsor with regard to Study related personal data. Institution shall continue to be an independent data controller of personal data processed by Institution with respect to the treatment of the Study Subject’s standard of care medical records. The Parties represent and warrant that they will comply with the provisions of Applicable Law relating to the confidentiality, privacy and security of such personal data. In addition, the Institution and Principal Investigator shall comply with the following provisions: 10. Ochrana osobních údajů a soukromí. Smluvní strany uznávají společný cíl zabezpečit všechny osobní údaje, zachovávat o nich mlčenlivost a chránit je před neoprávněným sdělením. Zadavatel bude nezávislým správcem údajů, pokud jde o jeho zpracování osobních údajů obsažených v osobních údajích souvisejících se studií hlášených hlavním zkoušejícím zadavateli nebo CRO. CRO působí jako zpracovatel údajů výhradně jménem zadavatele, pokud jde o osobní údaje související se studií. Zdravotnické zařízení bude nadále nezávislým správcem údajů pro osobní údaje zpracovávané zdravotnickým zařízením, pokud jde o nakládání se zdravotními záznamy studijních subjektů v rámci standardu péče. Smluvní strany prohlašují a zaručují, že budou dodržovat ustanovení platných zákonů týkajících se důvěrnosti, ochrany soukromí a zabezpečení takových osobních údajů. Kromě toho budou zdravotnické zařízení a hlavní zkoušející dodržovat následující ustanovení:
Personal Data Protection and Privacy. The Parties recognize a common goal of securing all personal data and holding such information in confidence and protecting it from unauthorized disclosure. The Parties represent and warrant that they will comply with the provisions of Applicable Law relating to the confidentiality, privacy and security of such personal data applicable to the territory of the Czech Republic, in particular Regulation (EU) No. 2016/679, the General Data Protection Regulation. 10.1. Within the scope of the Trial, Sponsor is the controller of the personal data of the subjects of the Trial, the Principal Investigator, and the Sponsor Research Staff (“personal data”). On the basis of this agreement and in relation to this agreement, personal data will also be processed by Institution and Principal Investigator both as controller (in particular when managing medical documentation) and to a certain extent as processor (in particular where personal data will be processed in accordance with the protocol for the purposes of the Trial). Each contracting party shall be responsible for their own processing of personal data and shall ensure that the personal data related to Trial subjects, Principal Investigator, and/or Research 10. Ochrana osobních údajů a soukromí. Strany jsou si vědomy společného cíle zabezpečení všech osobních údajů a zachování jejich důvěrnosti a ochrany před neoprávněným zveřejněním. Strany prohlašují a zaručují, že budou dodržovat všechna ustanovení platných zákonů upravujících důvěrnost, ochranu soukromí a zabezpečení těchto osobních údajů platných na území České republiky, a to zejména s nařízením (EU) č. 2016/679, Obecné nařízení o ochraně osobních údajů (GDPR). 10.1. V rámci klinického hodnocení je správcem osobních údajů subjektů klinického hodnocení, hlavního zkoušejícího a výzkumného personálu zadavatel („osobní údaje“). Na základě této smlouvy a v souvislosti s touto smlouvou budou osobní údaje zpracovávat rovněž zdravotnické zařízení a hlavní zkoušející, a to jako správci (zejména při vedení zdravotní dokumentace) a v určitém rozsahu také jako zpracovatelé (zejména tam, kde budou osobní údaje v souladu s protokolem zpracovávat pro účely klinického hodnocení). Každá smluvní strana bude odpovědná za své vlastní zpracování osobních údajů a zajistí, aby osobní údaje týkající se subjektů klinického hodnocení, hlavního zkoušejícího a/nebo
Personal Data Protection and Privacy. The Parties recognize a common goal of securing all personal data and holding such information in confidence and protecting it from unauthorized disclosure. During and after the completion of the clinical trial, the Parties shall be required to observe the applicable regulatory requirements on the personal data protection when processing and transferring personal data to another country, in particular Articles 26, 27 and 45 of the Regulation (EU) 2016/679 of the European Parliament and of the Council of 27.4.2016 on the protection of natural persons with regard to the processing of personal data and on the free movement of such data, and Act No. 110/2019 Coll., on processing of personal data and related applicable regulatory requirements. Sponsor shall be an independent data controller with respect to its processing of personal data contained in the Trial related personal data reported by Provider to Sponsor or CRO. The CRO is acting as a data processor solely on behalf of the Sponsor with regard to Trial related personal data. Provider shall continue to be an independent data controller of personal data processed by Provider with respect to the treatment of the Trial Subject’s standard of care medical records. specified in the medical documentation. He is also the administrator of personal data resulting from the performed clinical trial, which he passes on to the sponsor. The Parties represent and warrant that they will comply with the provisions of Applicable Law relating to the confidentiality, privacy and security of such personal data. In addition, the Provider shall comply with the following provisions: 8.1
Personal Data Protection and Privacy. The Parties recognize a common goal of securing all personal data and holding such information in confidence and protecting it from unauthorized disclosure. During and after the completion of the clinical trial, the Parties shall be required to observe the applicable regulatory requirements on the personal data protection when processing and transferring personal data to another country, in particular Articles 26, 27 and 45 of the Regulation (EU) 2016/679 of the European Parliament and of the Council of 27.4.2016 on the protection of natural persons with regard to the processing of personal data and on the free movement of such data, and Act No. 110/2019 Coll., on processing of personal data and related applicable regulatory requirements.The Parties represent and warrant that they will comply with the provisions of Applicable Law relating to the confidentiality, privacy and security of such personal data. In addition, the Institution shall comply with the following provisions: 8.1.
Personal Data Protection and Privacy. Parties agree that the Sponsor is acting as the Data Controller in respect of the pseudonymized Personal Data of the Trial subjects obtained under the Informed Consent Form, as well as the Personal Data of the Investigator and the employees of the Institution obtained under this Agreement for Trial purposes, and has assigned as Processor under this Agreement CRO. The Institution is acting as the Data Controller in respect of any medical records obtained by the Investigator from the Study subjects, the Study encryption key, and any other personal data the Investigator has gathered or generated in the course of the Study for the purposes of his of independent medical opinion in accordance with the Study Protocol. 10. Ochrana osobních údajů a soukromí. Strany souhlasí, že Zadavatel jedná jako Správce údajů ve vztahu ke kódovaným Osobním údajům subjektů hodnocení získaným v souladu s Formulářem informovaného souhlasu a Osobním údajům Hlavního zkoušejícího a zaměstnanců Zdravotnického zařízení získaným dle této Smlouvy, a pověřil dle této Smlouvy CRO jako zpracovatele. Zdravotnické zařízení jedná jako Správce údajů ve vztahu k jakýmkoli zdravotním záznamům, které Hlavní zkoušející získal od subjektů hodnocení, klíči pro kódování pro tuto studii a jakýmkoli dalším osobním údajům, které Hlavní zkoušející shromáždil nebo vygeneroval v průběhu Studie pro účely jeho 10.1. Parties undertake to establish and implement throughout the duration of this Agreement the appropriate operating, technical and organizational measures under applicable legislation (including the EU Regulation 2016/679, General Data Protection Regulation) to protect the personal data being gathered and processed for study-related purposes against unlawful destruction, alteration, unauthorized disclosure, access or any other unlawful operations with them. 10.2. In the event of the clinical Trial site (i.e. the Institution and the Principal Investigator) processing the relevant personal data of the Trial subjects exclusively for Trial-related purposes and in accordance with Sponsor’s instructions, it will be a Data Processor under the applicable personal data protection legislation. 10.3. The CRO and/or Sponsor (as applicable) has the right to access and use of the clinical trial data entry and processing system (eCRF) used on the Trial and that such access and use will not, to its current knowledge, infringe any third party rights 10.4. Parties undertake to inform each other promptly of any discover...
Personal Data Protection and Privacy. The POTENTIAL PURCHASER expressly agrees that its personal and private data are used by BESTVALUE to customize and enhance communication, i.e. through letters, e-mails or phone calls that the POTENTIAL PURCHASER expressly agrees to receive from BESTVALUE. BESTVALUE undertakes not to use the POTENTIAL PURCHASER’s personal data for purposes other than the purposes provided for in the recitals of this Agreement. BESTVALUE commits not to communicate or disclose, in any form, personal data related to the POTENTIAL PURCHASER, (i) unless the POTENTIAL PURCHASER has given its prior written agreement; (ii) except to the company or person which may acquire the COMPANY’s shares and/or assets; or (iii) except to jurisdictional authorities that may require access to the said data. The POTENTIAL PURCHASER has the right, at any time, to require any modification, amendment or withdrawal of its personal data from the BESTVALUE database, and the immediate cessation of receiving any further e- mails and/or other communication from BESTVALUE.
