Study Subject Medical Information Sample Clauses

Study Subject Medical Information. The Sponsor may access the Study Documents during regular business hours, upon reasonable advance notice to the Institution. The Sponsor shall comply with Applicable Law regarding the confidentiality of Study Subjects’ medical records and other health information, shall hold the Study Subjects’ personal identifying information in confidence, and shall act in accordance with the Informed Consents. Subject to the foregoing, the Sponsor may copy Institution records containing such information to the extent permitted by Applicable Law and the express authorization of Informed Consents from relevant Study Subjects. Institution acknowledges that Sponsor may disclose Study Documents to its drug development partners, other clinical investigators in the Study, the FDA and foreign regulatory 2.3 Zdravotní informace subjektů studie. Zadavatel může mít přístup k dokumentům studie během běžné pracovní doby, na základě přiměřeného předchozího oznámení zdravotnickému zařízení. Zadavatel bude dodržovat požadavky příslušných zákonů, které se týkají důvěrnosti zdravotních záznamů subjektů studie a jiných zdravotních informací, bude zachovávat důvěrnost informací subjektů studie, které umožňují jejich osobní identifikaci, a bude jednat v souladu s informovanými souhlasy. Za výše uvedených podmínek může zadavatel kopírovat záznamy zdravotnického zařízení, které obsahují tyto informace, v rozsahu povoleném příslušnými zákony a odpovídajícím oprávnění v informovaných souhlasech od příslušných subjektů studie. Zdravotnické zařízení bere na vědomí, že zadavatel může zpřístupnit dokumenty agencies. studie svým partnerům xxx xxxxxx xxxxxx, xxxxxxxx xxxxxxxxx zkoušejícím v rámci studie, úřadu FDA a zahraničním kontrolním úřadům.
Sample 1
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Study Subject Medical Information. The Sponsor may access the Study Materials during regular business hours, upon reasonable advance notice to the Institution. The Sponsor shall comply with Applicable Law regarding the confidentiality of Study Subjects’ medical records and other health information, shall hold the Study Subjects’ personal identifying information in confidence, and shall act in accordance with the Informed Consents. Subject to the foregoing, the Sponsor may copy Institution records containing such information to the extent permitted by Applicable Law and the express authorization of Informed Consents from relevant Study Subjects. Institution acknowledges that Sponsor may disclose Study Materials to its drug development partners, other clinical investigators in the Study, the FDA and other competent regulatory agencies. During monitoring/auditing, the legal obligations of the Institution shall be respected, especially the obligation of confidentiality and personal data protection, as well as protection of trade secrets of the Institution. The Sponsor shall be responsible for compliance with confidentiality requirements relating to such information of 2.3 Zdravotní informace subjektů studie. Zadavatel může mít přístup k materiálům studie během běžné pracovní doby, na základě přiměřeného předchozího oznámení zdravotnickému zařízení. Zadavatel bude dodržovat požadavky příslušných zákonů, které se týkají důvěrnosti zdravotních záznamů subjektů studie a jiných zdravotních informací, bude zachovávat důvěrnost informací subjektů studie, které umožňují jejich osobní identifikaci, a bude jednat v souladu s informovanými souhlasy. Za výše uvedených podmínek může zadavatel kopírovat záznamy zdravotnického zařízení, které obsahují tyto informace, v rozsahu povoleném příslušnými zákony a odpovídajícím oprávnění v informovaných souhlasech od příslušných subjektů studie. Zdravotnické zařízení bere na vědomí, že zadavatel může zpřístupnit materiály studie svým partnerům xxx xxxxxx xxxxxx, xxxxxxxx xxxxxxxxx zkoušejícím v rámci studie, úřadu FDA a jiným příslušným kontrolním úřadům. V rámci monitorování/auditu budou respektovány zákonné povinnosti zdravotnického zařízení, především povinnost mlčenlivosti a ochrany osobních údajů, a dále ochrana obchodního tajemství zdravotnického zařízení. Za dodržování požadavků mlčenlivosti týkajících se těchto informací ze strany osob provádějících audit persons performing the audit. Access for monitoring/auditing purposes shall be allowed only into rooms i...
Sample 1
Study Subject Medical Information. The Sponsor may access the Study Documents during regular business hours, upon reasonable advance notice to the Institution/Principal Investigator. The Sponsor shall comply with Applicable Law regarding the confidentiality of Study Subjects’ medical records and other health information, shall hold the Study Subjects’ personal identifying information in confidence, and shall act in accordance with the Informed Consents and the HIPAA Authorizations (as defined in Section 9.5). Subject to the foregoing, the Sponsor may 2.
Sample 1

Related to Study Subject Medical Information

  • Medical Information Throughout the Pupil's time as a member of the School, the School Medical Officer shall have the right to disclose confidential information about the Pupil if it is considered to be in the Pupil's own interests or necessary for the protection of other members of the School community. Such information will be given and received on a confidential, need-to-know basis.

  • Technical Information The Employer agrees to provide to the Union such information that is available relating to employees in the bargaining unit, as may be required by the Union for collective bargaining purposes.

  • INITIAL INFORMATION § 1.1 This Agreement is based on the Initial Information set forth in this Section 1.1. (For each item in this section, insert the information or a statement such as “not applicable” or “unknown at time of execution.”)

  • Trade Secrets, Commercial and Financial Information It is expressly understood that Mississippi law requires that the provisions of this contract which contain the commodities purchased or the personal or professional services provided, the price to be paid, and the term of the contract shall not be deemed to be a trade secret or confidential commercial or financial information and shall be available for examination, copying, or reproduction.

  • Contractor Information The Contractor will provide up to date information for each of the following in the form and manner specified by OGS:

  • Research, Science and Technology Cooperation 1. The aims of cooperation in research, science and technology, carried out in the mutual interest of the Parties and in compliance with their policies, will be: (a) to build on existing agreements already in place for cooperation on research, science and technology; (b) to encourage, where appropriate, government agencies, research institutions, universities, private companies and other research organizations in the Parties to conclude direct arrangements in support of cooperative activities, programs or projects within the framework of this Agreement, specially related to trade and commerce; and (c) to focus cooperative activities towards sectors where mutual and complementary interests exist, with special emphasis on information and communication technologies and software development to facilitate trade between the Parties. 2. The Parties will encourage and facilitate, as appropriate, the following activities including, but not limited to:

  • INFORMATION TECHNOLOGY The following applies to all contracts for information technology commodities and contractual services. “Information technology” is defined in section 287.012(15), F.S., to have the same meaning as provided in section 282.0041, F.S.

  • Patient Information Each Party agrees to abide by all laws, rules, regulations, and orders of all applicable supranational, national, federal, state, provincial, and local governmental entities concerning the confidentiality or protection of patient identifiable information and/or patients’ protected health information, as defined by any other applicable legislation in the course of their performance under this Agreement.

  • Clinical 2.1 Provides comprehensive evidence based nursing care to patients including assessment, intervention and evaluation.

  • Confidentiality of Contractor Information The Contractor acknowledges and agrees that this Contract and any and all Contractor information obtained by the State in connection with this Contract are subject to the State of Vermont Access to Public Records Act, 1 V.S.A. § 315 et seq. The State will not disclose information for which a reasonable claim of exemption can be made pursuant to 1 V.S.A. § 317(c), including, but not limited to, trade secrets, proprietary information or financial information, including any formulae, plan, pattern, process, tool, mechanism, compound, procedure, production data, or compilation of information which is not patented, which is known only to the Contractor, and which gives the Contractor an opportunity to obtain business advantage over competitors who do not know it or use it. The State shall immediately notify Contractor of any request made under the Access to Public Records Act, or any request or demand by any court, governmental agency or other person asserting a demand or request for Contractor information. Contractor may, in its discretion, seek an appropriate protective order, or otherwise defend any right it may have to maintain the confidentiality of such information under applicable State law within three business days of the State’s receipt of any such request. Contractor agrees that it will not make any claim against the State if the State makes available to the public any information in accordance with the Access to Public Records Act or in response to a binding order from a court or governmental body or agency compelling its production. Contractor shall indemnify the State for any costs or expenses incurred by the State, including, but not limited to, attorneys’ fees awarded in accordance with 1 V.S.A. § 320, in connection with any action brought in connection with Contractor’s attempts to prevent or unreasonably delay public disclosure of Contractor’s information if a final decision of a court of competent jurisdiction determines that the State improperly withheld such information and that the improper withholding was based on Contractor’s attempts to prevent public disclosure of Contractor’s information. The State agrees that (a) it will use the Contractor information only as may be necessary in the course of performing duties, receiving services or exercising rights under this Contract; (b) it will provide at a minimum the same care to avoid disclosure or unauthorized use of Contractor information as it provides to protect its own similar confidential and proprietary information; (c) except as required by the Access to Records Act, it will not disclose such information orally or in writing to any third party unless that third party is subject to a written confidentiality agreement that contains restrictions and safeguards at least as restrictive as those contained in this Contract; (d) it will take all reasonable precautions to protect the Contractor’s information; and (e) it will not otherwise appropriate such information to its own use or to the use of any other person or entity. Contractor may affix an appropriate legend to Contractor information that is provided under this Contract to reflect the Contractor’s determination that any such information is a trade secret, proprietary information or financial information at time of delivery or disclosure.

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