EU GDPR Sample Clauses

EU GDPR. In relation to Personal Data that is protected by the EU GDPR, the EU SCCs are incorporated and will apply completed as follows: Module 2 of the EU SCCs applies between Customer as "data exporter" and ClickDimensions as "data importer" on the following basis: (i) in Clause 7, the optional docking clause will apply, (ii) in Clause 9, Option 2 will apply, and the time period for prior notice of Sub-Processor changes shall be as set out in Section 11(c) of this Addendum, (iii) in Clause 11, the optional language shall not apply, (iv) in Clause 17, Option 1 will apply, and the EU SCCs will be governed by , (v) in Clause 18(b), disputes shall be resolved before the courts of , (vi) Annex 1 to the EU SCCs will be deemed to incorporate Schedule 1 to this Addendum and (vii) Annex 2 to the EU SCCs will be deemed to incorporate Schedule 2 of this Addendum.
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EU GDPR. You have the right to information and may request a copy of your data processed by us. • Article 16 EU-GDPR: You have the right to make corrections and make sure that your data is complete.
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EU GDPR. You have the right to object at any time to the processing of your relevant data. • Article 7 EU-GDPR, you have the right to withdraw consent to the processing of your personal data at any time. When you withdraw your consent, the personal data used between your acquiescence to consent and your withdrawal of consent is lawfully used data. Herewith I agree to the processing of my personal data in the above scope and for the purposes stated therein, by the responsible persons. I have received the information required under the EU General Data Protection Regulations (EU-GDPR). I am content with the conditions as well as the rights granted to me under this agreement. Date Signature of Research Participant Date Signature of Researcher Attachment 5: Researcher Commitment Form Promoting Research on Digitalisation in Emerging Powers and Europe Towards Sustainable Development How to interpret this form: This form is to be read and signed by the Researcher. This form is the Researcher's commitment to ethical research practices. Please make yourself knowledgeable of the PRODIGEES Data Protection Policy, as well as the European Union General Data Protection Regulations (EU-GDPR). Please return this signed commitment to the PRODIGEES project manager and your host supervisor.
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EU GDPR. If Company creates, accesses, transmits or stores Villanova Data that is subject to the European Union’s Regulation (EU) 2016/679 (“Regulation on the protection of natural persons with regard to the processing of personal data and on the free movement of such data,” or the “EU GDPR”), Villanova and Company agree as follows: 1. For purposes of this Section, the terms Process/Processor/Processing, Personal Data, Third Country, International Organization, Member State, and Data Subject shall be defined and construed as set forth in the EU GDPR. 2. Company agrees to implement appropriate technical and organizational measures in compliance with the requirements of the EU GDPR. 3. Company shall not engage another Processor without prior specific or general written authorization of Villanova. If a general written authorization is provided, Company shall inform Xxxxxxxxx of any intended changes concerning the addition or replacement of other Processors and provide Villanova the opportunity to object to such changes. If any other Processor is engaged, Company shall ensure that the Processor shall comply with all data protection obligations as set forth herein and otherwise required by the EU GDPR. Company shall remain fully liable to Villanova for the performance of any other Processor’s obligations. 4. Company shall only engage in Processing (including with respect to subject matter, duration, nature and purpose of the Processing) as necessary to carry out its obligations under the Agreement and as set forth in greater detail therein. Company shall reasonably assist Villanova in carrying out any and all of its obligations under the EU GDPR, as applicable and within the scope of the Agreement. Company shall Process Personal Data only on documented instructions from Villanova, including with regard to transfers of Personal Data to a Third Country of International Organization, unless required to do so by European Union or Member State law to which Company is subject; in such a case, Company shall inform Villanova of that legal requirement before Processing, unless that law prohibits such information on important grounds of public interest. Company shall immediately inform Villanova if, in its opinion, an instruction infringes the EU GDPR or other European Union or Member State data protection provisions. 5. Company shall ensure that all personal authorized to Process the Personal Data have committed themselves to confidentiality or are under an appropriate statutory...
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EU GDPR. Supplier agrees to comply with the provisions of the GDPR at the University’s request, if practicable, including but not limited: collecting the minimum amount of information necessary to perform its duties, limiting retention of personal data as specified therein, deleting information specific to individuals upon request – except as necessary to perform its job function, and responding to requests from the instructor for the status of individuals’ data. Supplier shall assume responsibility for interacting with any and all individual inquiries to Supplier constituting a request under the GDPR.
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EU GDPR. The customer names a legitimate point of contact who is entitled to give instructions according to this DPA and informs about any changes in a known way.
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EU GDPR. Totaljobs shall inform the customer without undue delay if a data subject contacts Totaljobs directly for the purpose of providing access, rectification, erasure or restricting the processing of their personal data. Totaljobs shall support the customer in carrying out data protection impact assessments pursuant to Art. 35 EU GDPR and the resulting consultation of the supervisory authority pursuant to Art. 36 EU GDPR to the necessary extent. Totaljobs shall support the customer with regard to compliance with reporting and notification obligations in the event of data protection breaches within the meaning of Artt. 33 and 34 EU GDPR.
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Related to EU GDPR

  • GDPR SAP and Customer agree that it is each party’s responsibility to review and adopt requirements imposed on Controllers and Processors by the General Data Protection Regulation 2016/679 (“GDPR”), in particular with regards to Articles 28 and 32 to 36 of the GDPR, if and to the extent applicable to Personal Data of Customer/Controllers that is processed under the DPA. For illustration purposes, Appendix 3 lists the relevant GDPR requirements and the corresponding sections in this DPA.

  • DPR A DPR is 1/365th of an APR, rounded to one tenthousandth of a percentage point. Your DPRs are shown in How Rates and Fees Work on page 2 of Part 1.

  • Technology Research Analyst Job# 1810 General Characteristics

  • Marketing Plan The MCOP shall submit an annual marketing plan to ODM including all planned activities for promoting membership in or increasing awareness of the MCOP. The marketing plan submission shall include an attestation by the MCOP that the plan is accurate and is not intended to mislead, confuse, or defraud the eligible individuals or ODM.

  • TECHNICAL EVALUATION (a) Detailed technical evaluation shall be carried out by Purchase Committee pursuant to conditions in the tender document to determine the substantial responsiveness of each tender. For this clause, the substantially responsive bid is one that conforms to all the eligibility and terms and condition of the tender without any material deviation. The Institute’s determination of bid’s responsiveness is to be based on the contents of the bid itself without recourse to extrinsic evidence. The Institute shall evaluate the technical bids also to determine whether they are complete, whether required sureties have been furnished, whether the documents have been properly signed and whether the bids are in order. (b) The technical evaluation committee may call the responsive bidders for discussion or presentation to facilitate and assess their understanding of the scope of work and its execution. However, the committee shall have sole discretion to call for discussion / presentation. (c) Financial bids of only those bidders who qualify the technical criteria will be opened provided all other requirements are fulfilled. (d) AIIMS Jodhpur shall have right to accept or reject any or all tenders without assigning any reasons thereof.

  • Tests and Preclinical and Clinical Trials The preclinical studies and clinical trials conducted by or, to the Company’s knowledge, on behalf of the Company, that are described in the Registration Statement, the Pricing Disclosure Package and the Prospectus, as applicable, and are intended to be submitted to the U.S. Food and Drug Administration (the “FDA”) or other comparable government entities, were and, if still ongoing, are being conducted in all material respects in accordance with experimental protocols, procedures and controls pursuant to accepted professional scientific standards and all Authorizations and Applicable Laws, including, without limitation, current Good Clinical Practices and Good Laboratory Practices and any applicable rules and regulations of the jurisdiction in which such trials and studies are being conducted; the descriptions of the results of such studies and trials contained in the Registration Statement, the Pricing Disclosure Package and the Prospectus are, to the Company’s knowledge, accurate and complete in all material respects and fairly present the data derived from such studies and trials; except to the extent disclosed in the Registration Statement, the Pricing Disclosure Package and the Prospectus, the Company is not aware of any studies or trials, the results of which the Company believes reasonably call into question the study or trial results described or referred to in the Registration Statement, the Pricing Disclosure Package and the Prospectus when viewed in the context in which such results are described and the clinical stage of development; and, except to the extent disclosed in the Registration Statement, the Pricing Disclosure Package or the Prospectus, the Company has not received any written notices or written correspondence from the FDA or any governmental entity requiring the termination or suspension of any preclinical studies or clinical trials conducted by or on behalf of the Company, other than ordinary course communications with respect to modifications in connection with the design and implementation of such trials, copies of which communications have been made available to you.

  • Commercialization Plan (a) Not later than three [***] after submission of Regulatory Filings for each Product in each country of the Territory, Licensee will provide to the JCC for review its initial Commercialization Plan for each Product for each country in the Territory. Such initial Commercialization Plan will describe Licensee’s plans for activities to be conducted for such Product for such country. Each Commercialization Plan shall include the details of obligations to be performed by Licensee to achieve the specific activities that are applicable to the stage of [***] Certain information in this document has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions. Commercialization (e.g., pre-launch, launch planning, launch, or post-launch) of the applicable Product during the time period covered by such Commercialization Plan and subsequent time periods. (b) Prior to the First Commercial Sale for such Product in such country, Licensee will provide to the JCC for review an updated Commercialization Plan for such Product for such country. Such updated Commercialization Plan will include, but not be limited to, Licensee’s updated plans for activities to be conducted for such Product for such country prior to launch as well as activities to be conducted in connection with such launch. (c) Promptly after each anniversary of the First Commercial Sale of such Product during the Term, Licensee will provide to the JCC for review updated Commercialization Plans for such Product for such country. Such further updated Commercialization Plan will include, but not be limited to, Licensee’s plans for Commercialization activities for such Product and such country for the twelve (12) month period following the date of delivery of such Commercialization Plan. No Commercialization Plan may be implemented by Licensee if [***]. Each Commercialization Plan shall be consistent with and shall not contradict the terms of this Agreement [***], and in the event of any inconsistency between the Commercialization Plan and this Agreement, the terms of this Agreement shall prevail. Notwithstanding the foregoing, if a [***], Licensee shall [***] and shall promptly [***].

  • MINISTRY/SCHOOL BOARD INITIATIVES ETFO will be an active participant in the consultation process to develop a Ministry of Education PPM regarding Ministry/School Board Initiatives.

  • Commercial Milestones (a) Within [*****] calendar days after the end of the first Calendar Year in which aggregate annual Net Sales for that Calendar Year for the Licensed Product in the Territory reach any threshold indicated in the Commercial Milestone Events listed below, EverInsight shall notify VistaGen of the achievement of such Commercial Milestone Event and VistaGen shall invoice EverInsight for the corresponding non-refundable, non-creditable Milestone Payment set forth below and EverInsight shall remit payment to VistaGen within [*****] Business Days after the receipt of the invoice, as described in Section 8.6 (Currency; Exchange Rate; Payments). Annual Net Sales Milestones for Licensed Product Milestone Payments (in Dollars) (each a “Commercial Milestone Event”): (1). [*****] (2). [*****] (3). [*****] (4). [*****] (5). [*****] (b) For the purposes of determining whether a Net Sales Milestone Event has been achieved, Net Sales of Licensed Product(s) in the Territory shall be aggregated. For clarity, the annual Net Sales Milestone Payments set forth in this Section 8.3 (Commercial Milestones) shall be payable only once, upon the first achievement of the applicable Commercial Milestone Event, regardless of how many times such Commercial Milestone Event is achieved. (c) If a Commercial Milestone Event in Section 8.3 (Commercial Milestones) is achieved and payment with respect to any previous Commercial Milestone Event in Section 8.3 has not been made, then such previous Commercial Milestone Event shall be deemed achieved and EverInsight shall notify VistaGen within fifteen (15) calendar days of such achievement. VistaGen shall then invoice EverInsight for such unpaid previous Commercial Milestone Event(s) and EverInsight shall pay VistaGen such unpaid previous milestone payment(s) within thirty (30) Business Days of receipt of such invoice. (d) In the event that, VistaGen believes any Commercial Milestone Event under Section 8.3(a) has occurred but EverInsight has not given VistaGen the notice of the achievement of such Commercial Milestone Event, it shall so notify EverInsight in writing and shall provide to EverInsight data, documentation or other information that supports its belief. Any dispute under this Section 8.3(d) (Commercial Milestones - subsection (d)) that relates to whether or not a Commercial Milestone Event has occurred shall be referred to the JSC to be resolved in accordance with ARTICLE 3 (Governance) and shall be subject to resolution in accordance with Section 14.10 (Dispute Resolution). The Milestone Payments made for each Commercial Milestone Event shall be non-creditable and non-refundable.

  • Development Plan document specifying the work program, schedule, and relevant investments required for the Development and the Production of a Discovery or set of Discoveries of Oil and Gas in the Concession Area, including its abandonment.

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