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) 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. (c) Povinnosti zdravotnického zařízení (iii) Zdravotnické zařízení souhlasí s xxx, že výzkumný personál vynaloží své nejlepší úsilí na přesné a efektivní provádění práce požadované podle této smlouvy, přičemž toto úsilí zejména zahrnuje položky (i) až (iv) uvedené v odstavci 3(b) shora. (iv) Zdravotnické zařízení zaručuje, že ve zdravotnickém zařízení je k dispozici příslušná nezbytná a adekvátní vybavenost včetně zařízení nezbytného (s výjimkou toho, které poskytne zdravotnickému zařízení Chiltern jménem zadavatele) pro provádění studie (odpovídající prostory pro fyzikální vyšetření podle protokolu, odběry krve). 4.
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 which do not maintain as stringent data protection standards as contemplated herein. (b) Covance may make available such Personal Information to affiliated companies of Sponsor and/or Covance, legal and regulatory agencies and authorities. (c) Investigator warrants that it has obtained the necessary consents of the Research Staff, in accordance with applicable data protection laws for the collection, processing, storage and transfer of their Personal Information for the above mentioned purposes. 6.
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 Investigator agree to comply with the terms of the DPA in relation to Data Protection. (b) Covance may make available such Personal Information to affiliated companies of Sponsor and/or Covance, legal and regulatory agencies and authorities. (c) Investigator warrants that it has obtained the necessary consents of the Research Staff, in accordance with applicable data protection laws for the collection, processing, storage and transfer of their Personal Information for the above mentioned purposes. 6. CONFIDENTIALITY (a) Institution and Investigator shall not, and Investigator shall ensure that Research Staff shall not disclose to any third party or use for any purposes other than for the performance of the Study any data, records or other information disclosed to Institution and Investigator by Covance, Sponsor, Sponsor’s independent contractors or generated as a result of this Study (hereinafter, collectively "Information") without the prior written consent of Sponsor. Such Information shall remain the confidential and proprietary property of Sponsor and shall be disclosed only to Research Staff bound by obligations of confidentiality consistent with this Agreement who have a “need to know” for the performance of the Study. The obligation of nondisclosure shall not apply to the following Information: (i) Information that is or becomes publicly available through no fault of Institution, Investigator or Research Staff; (ii) Information that is disclosed to Institution, Investigator, and/or Research Staff by a third party legally entitled to disclose such information in a non-confidential fashion; (iii) Information that is already known to Institution, Investigator, and/or Research Staff as shown by its prior written records; (iv) Information required to be disclosed to a government authority or by order of a court of competent jurisdiction, provided that to the extent permissible by law (i) such disclosure is patient to all applicable governmental or judicial Zdravotnické zařízení a Zkoušející musí nábor zastavit v souladu s předchozími písemnými pokyny. 5.
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
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 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. (c) Investigator warrants that it has obtained the necessary consents of the Research Staff, in accordance with applicable data protection laws for the collection, processing, storage and transfer of their Personal Information for the above mentioned purposes. 6.
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 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

Related to PERSONAL DATA OF INVESTIGATOR AND RESEARCH STAFF

  • Personal Data, Confidentiality, Recording of Telephone Calls and Records 22.1. The Company may collect client information directly from the Client (in his completed Account Opening Application Form or otherwise) or from other persons including, for example, the credit reference agencies, fraud prevention agencies, banks, other financial institutions, third authentication service providers and the providers of public registers.

  • Customer’s Processing of Personal Data Customer shall, in its use of the Services, Process Personal Data in accordance with the requirements of Data Protection Laws and Regulations. For the avoidance of doubt, Customer’s instructions for the Processing of Personal Data shall comply with Data Protection Laws and Regulations. Customer shall have sole responsibility for the means by which Customer acquired Personal Data.

  • Processing Personal Data 40.1. The Company is the data controller in the relevant jurisdiction. You hereby acknowledge and agree to the collection and processing of personal data provided by you in connection with the opening of a trading account for the purpose of performing our obligations under these Terms and Conditions and for administering the relationship between you and us.

  • Access to Personal Information by Subcontractors Supplier agrees to require any subcontractors or agents to which it discloses Personal Information under this Agreement or under any SOW to provide reasonable assurance, evidenced by written contract, that they will comply with the same or substantially similar confidentiality, privacy and security obligations with respect to such Personal Information as apply to Supplier under this Agreement or any SOW. Supplier shall confirm in writing to DXC that such contract is in place as a condition to DXC’s approval of use of a subcontractor in connection with any SOW. Upon request of DXC, Supplier will provide to DXC a copy of the subcontract or an extract of the relevant clauses. Supplier shall ensure that any failure on the part of any subcontractor or agent to comply with the Supplier obligations under this Agreement or any SOW shall be grounds to promptly terminate such subcontractor or agent. If during the term of this Agreement or any SOW, DXC determines, in its exclusive discretion, that any Supplier subcontractor or agent cannot comply with the Supplier obligations under this Agreement or with any SOW, then DXC may terminate this Agreement in whole or in part (with respect to any SOW for which such subcontractor or agent is providing services), if not cured by Supplier within the time prescribed in the notice of such deficiency.

  • Services and Third Party Materials A. The tvOS Software may enable access to Apple’s iTunes Store, App Store, Game Center, iCloud and other Apple and third party services, and web sites (collectively and individually, “Services”). Such Services may not be available in all languages or in all countries. Use of these Services requires Internet access and use of certain Services may require an Apple ID, may require you to accept additional terms and may be subject to additional fees. By using this software in connection with an Apple ID, or other Apple Service, you agree to the applicable terms of service for that Service, such as the latest iTunes Store Terms and Conditions, which you may access and review at xxxx://xxx.xxxxx.xxx/legal/itunes/ ww/.

  • Personal Data Processing 2.1 The Processor shall process Personal Data only on the basis of corresponding recorded orders from the Controller.

  • Employee Access to Personnel File An employee shall have the right to read and review his/her personnel file on reasonable notice and by written request to the Human Resources Manager. An employee may request and shall receive a copy of any record or document contained in the employee’s personnel file.

  • 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).

  • 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.

  • HOW WE MAY USE YOUR PERSONAL INFORMATION 8.1 We will use the personal information You provide to Us to:

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