Data protection Clausole campione

Data protection. 11.1 In executing the contractual activities the Parties shall treat all the personal data they receive for any reason in relation to the clinical Trial in accordance with the objectives of the foregoing articles and in conformity with the provisions of Regulation (EU) 2016/679 of the European Parliament and Council of 27 April 2016 (GDPR), and with the related provisions of Consiglio del 27 aprile 2016 (“GDPR”), nonché dalle correlate disposizioni legislative e amministrative nazionali vigenti, con le loro eventuali successive modifiche e/o integrazioni (di seguito, collettivamente, “Leggi in materia di Protezione dei dati”) nonché degli eventuali regolamenti degli Enti. 11.2 I termini utilizzati nel presente articolo, nel Contratto, nella documentazione di informativa e consenso e in ogni altro documento utilizzato per le finalità della sperimentazione clinica devono essere intesi e utilizzati secondo il significato a essi attribuito nell’Allegato B. 11.3 L’Ente e il Promotore si qualificano come autonomi titolari del trattamento dei rispettivi dati ai sensi dell’art. 4 paragrafo 7 del GDPR. Ciascuna delle Parti provvederà a propria cura e spese, nell’ambito del proprio assetto organizzativo, alle eventuali nomine di Responsabili del trattamento e attribuzione di funzioni e compiti a soggetti designati, che operino sotto la loro autorità, ai sensi del GDPR e della normativa vigente. Lo Sponsor sarà il responsabile del trattamento dei dati dei soggetti dello Studio e del Personale di Ricerca raccolti nell'esecuzione dello Studio. L'Istituzione sarà il responsabile del trattamento dei dati dei soggetti law and orders of national administrations, including any subsequent amendments (collectively the “Data Protection Laws”) as well as any regulations of the Entities. 11.2 The terms used in this article, in this Agreement, in the informed consent documents and in any other documents used for the purposes of the Trial shall be construed and utilized in accordance with the meanings given in Annex B. 11.3 The Entity and Sponsor are independent data controllers of its respective data for the purposes of article 4 paragraph 7 of the GDPR. Each of the Parties will arrange at its own expense, as part of its organizational structure, for the appointment of Data Processors and assignment of functions and tasks to designated subjects, who operate under their authority, in accordance with the GDPR and current legislation. The Sponsor shall be the controller of data of S...

Data protection. 11.1 In executing the contractual activities the Parties shall treat all the personal data they receive for any reason in relation to the Trial in accordance with the objectives of the foregoing articles and in conformity with the provisions of Regulation (EU) 2016/679 of the European Parliament and Council of 27 April 2016 (General Regulations for the Protection of Personal Data, hereinafter "GDPR"), and with the related provisions of law and orders of national administrations, including any subsequent amendments (collectively the “Data Protection Laws”). 11.2 The terms used in this article, in this Agreement, in the informed consent documents and in any other documents used for the purposes of the Trial shall be construed and utilised in accordance with the meanings given in Annex B. 11.3 The Entity and the Sponsor (or the CRO if the CRO manages every aspect of the Trial in place of the Sponsor, assuming the ownership of the related treatments) are independent data controllers for the purposes of article 4 paragraph 7 of the GDPR. (Omit the following paragraph if the CRO is managing every aspect of the Trial instead of the Sponsor, assuming the ownership of the related treatments). The CRO ____ is the Data Processor for the purposes of Article 28 GDPR in reference to the ownership of the Sponsor and/or the Entity. 11.4 For the purposes of the Trial, personal data relating to the following categories of data subject will be processed: persons taking part in the trial; persons operating on the Parties’ behalf. Such data subjects will be appropriately informed of the processing of their data. For the purposes of the Trial, the following types of personal data will be processed: the data referred to in article 4 paragraph 1 of the GDPR; data classified as “sensitive” – and in particular, data relating to health, sexual preferences and genetic data – referred to in Article 9 GDPR. Such data shall be processed in accordance with the principles of legality, fairness, transparency, adequacy, relevance and necessity as contained in Article 5 paragraph 1 of the GDPR. 11.5 The Sponsor may transmit the data to affiliates of the Promoter's group and to third parties operating on its behalf, even abroad, in countries outside the European Union that do not offer the same level of privacy protection guaranteed in Europe. In this case, the Sponsor undertakes that this transfer takes place only to countries considered safe by the European Commission or, in any case, accor...

Data protection. Le Parti nell’esecuzione delle attività previste dal presente Contratto si impegnano a trattare i dati 11.1 In executing the contractual activities the Parties shall treat all the personal data they receive personali, di cui vengano per qualsiasi motivo a conoscenza durante la Sperimentazione clinica, nel rispetto degli obiettivi di cui ai precedenti articoli e in conformità a quanto disposto dal Regolamento (UE) 2016/679 del Parlamento Europeo e del Consiglio del 27 aprile 2016, nonché dalle correlate disposizioni legislative e amministrative nazionali vigenti, con le loro eventuali successive modifiche e/o integrazioni (di seguito, collettivamente, “Leggi in materia di Protezione dei dati”), nonché degli eventuali regolamenti delle parti. for any reason in relation to the Trial in accordance with the objectives of the foregoing articles and in conformity with the provisions of Regulation (EU) 2016/679 of the European Parliament and Council of 27 April 2016, and with the related provisions of law and orders of national administrations, including any subsequent amendments (collectively the “Data Protection Laws”) as well as any regulations of the entities.

Data protection. In executing the contractual activities the Parties shall treat all the personal data they receive for any reason in relation to the clinical Trial in accordance with the objectives of the foregoing articles and in conformity with the provisions of Regulation (EU) 2016/679 of the European Parliament and Council of 27 April 2016 (“GDPR”),, and with the related provisions of law and orders of national administrations, including any subsequent amendments (collectively the “Data Protection Laws”) as well as any regulations of the entities

Data protection. Please note that EDA will not return applications to candidates. The personal information EDA requests from candidates will be processed in line with Regulation (EU) N° 2018/1725 of the European Parliament and of the Council of 23 October 2018 on the protection of natural persons with regard to the processing of personal data by the Union institutions, bodies, offices and agencies and on the free movement of such data, and repealing Regulation (EC) 45/2001 and Decision No.

Data protection. Le Parti nell’esecuzione delle attività previste dal presente Contratto si impegnano a trattare i dati personali, di cui vengano per qualsiasi motivo a conoscenza durante lo Studio, nel rispetto degli obiettivi di cui ai precedenti articoli e in conformità a quanto disposto dal Regolamento (UE) 2016/679 del Parlamento Europeo e del Consiglio del 27 aprile 2016, nonché dalle correlate disposizioni legislative e amministrative nazionali vigenti, con le loro eventuali successive modifiche e/o integrazioni (di seguito, collettivamente, “▇▇▇▇▇ in materia di Protezione dei dati”).

Data protection. 1.1 Both parties will comply with all applicable requirements of the Data Protection and Domestic Legislation. This Appendix is in addition to, and does not relieve, remove or replace, a party 's obligations or rights under the Data Protection Legislation. 1.2 The parties acknowledge that for the purposes of the Data Protection Legislation, the roles of Controller, Processor and/or Sub - Processor may be dependent on the services actually being provi ded by the Parties under the Agreement and/or the source of the personal data, amongst other factors, and, as such, these roles shall be assigned on a case by case basis as reflected in the Annex[es] to this Appendix. The provisions below shall apply to each Party as appropriate and in accordance with those Annexes. 1.3 Where both Parties are acting as independent Controllers, each Party agrees to comply with the requirements of the Data Protection Laws applicable to Controllers in respect of the Personal Data transferred pursuant to this Agreement. 1.4 The Controller will en sure that it has all necessary appropriate consents and notices in place to enable lawful transfer of the Personal Data to the Processor and/or lawful collection of the Personal Data by the Processor on behalf of the Controller for the duration and purpose s of this Agreement. 1.5 The Processor shall, in relation to any Personal Data processed in connection with the performance by the Processor of its obligations under this agreement: a) process that Personal Data only on the documented written instructions of the Controller which are set out in the Agreement unless the Processor is required by Applicable Law to otherwise process that Personal Data. Where the Processor is relying on Applicable Law as the basis for processing Personal Data, the Processor shall prompt ly notify the Controller of this before performing the processing required by the Applicable Law unless such Applicable Law prohibits the Processor from so notifying the Controller; b) ensure that it has in place appropriate technical and organisational measures, reviewed by the Controller, to protect against unauthorised or unlawful processing of Personal Data and against accidental loss or destruction of, or damage to, Personal Data, appropriate to the harm that might result from the unauthorised or unlawful processing or accidental loss, destruction or damage DEFINIZIONI 1. Titolare, Responsabile del trattamento, Interessato, Dati Personali, Violazione dei Dati Personali, t...

Data protection. Le Parti, nell’esecuzione delle attività previste dal presente Contratto, si impegnano a trattare i dati personali, di cui vengano per qualsiasi motivo a conoscenza durante la sperimentazione clinica, nel rispetto degli obiettivi di cui ai precedenti articoli e in conformità a quanto disposto dal Regolamento (UE) 2016/679 del Parlamento Europeo e del Consiglio del 27 aprile 2016 (“GDPR”), nonché dalle correlate disposizioni legislative e amministrative nazionali vigenti, con le loro eventuali successive modifiche e/o integrazioni (di seguito, collettivamente, “Leggi in materia di Protezione dei dati”) nonché degli eventuali regolamenti degli Enti. 11.1. In executing the contractual activities the Parties shall treat all the personal data they receive for any reason in relation to the clinical Trial in accordance with the objectives of the foregoing articles and in conformity with the provisions of Regulation (EU) 2016/679 of the European Parliament and Council of 27 April 2016 (GDPR), and with the related provisions of law and orders of national administrations, including any subsequent amendments (collectively the “Data Protection Laws”) as well as any regulations of the Entities.

Data protection. 11.1 In executing the contractual activities the Parties shall treat all the personal data they receive for any reason in relation to the clinical trial in accordance with the objectives of the foregoing articles and in conformity with the provisions of Regulation (EU) 2016/679 of the European Parliament and Council of 27 April 2016, and with the related provisions of law and orders of national administrations, including any subsequent amendments (collectively the “Data Protection Laws”). 11.2 The terms used in this article, in this Agreement, in the informed consent documents and in any other documents used for the purposes of the clinical trial shall be construed and utilised in accordance with the meanings given in Annex B. 11.3 The Entity and Sponsor are independent data controllers for the purposes of article 4 paragraph 17 of the GDPR. (Omit the following paragraph if the CRO is managing every aspect of the Trial instead of the Sponsor, assuming the ownership of the related treatments). The CRO ____ is the Data Processor for the purposes of Article 28 GDPR in reference to the ownership of ___. 11.4 For the purposes of the Trial, personal data relating to the following categories of data subject will be processed: persons taking part in the trial; persons operating on the Parties’ behalf. Such data subjects will be appropriately informed of the processing of their data. For the purposes of the Trial, the following types of personal data will be processed: the data referred to in article 4 paragraph 1 of the GDPR; data classified as “sensitive” – and in particular, data relating to health, sexual preferences and genetic data – referred to in Article 9 GDPR. Such data shall be processed in accordance with the principles of legality, fairness, transparency, adequacy, relevance and necessity as contained in Article 5 paragraph 1 of the GDPR.