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Confidentiality Agreement For Research Participants
"I need a Confidentiality Agreement for Research Participants for a medical research study at Manila General Hospital, with specific provisions for handling sensitive health data and provisions for data sharing with our international research partners in Singapore."
1. Parties: Identifies the research institution/organization and the research participant
2. Background: Explains the context of the research project and the need for confidentiality
3. Definitions: Defines key terms including 'Confidential Information', 'Research Project', 'Personal Data', and other relevant terms
4. Purpose of Disclosure: Explains why confidential information will be shared with the participant and how it will be used
5. Scope of Confidential Information: Clearly defines what information is considered confidential within the research context
6. Confidentiality Obligations: Details the participant's obligations to maintain confidentiality of research information
7. Data Privacy Compliance: Addresses compliance with the Data Privacy Act of 2012 and related regulations
8. Duration of Confidentiality: Specifies how long the confidentiality obligations will remain in effect
9. Return or Destruction of Confidential Information: Procedures for handling confidential information after participation ends
10. Breach and Consequences: Outlines what constitutes a breach and the consequences thereof
11. Governing Law and Jurisdiction: Specifies Philippine law as governing law and relevant jurisdiction
1. Health Data Provisions: Additional provisions for research involving health or medical data
2. Third Party Disclosure: Provisions for cases where information might need to be shared with other researchers or institutions
3. Publication Rights: Provisions regarding the participant's rights and restrictions regarding publication of research-related information
4. Intellectual Property Rights: Provisions dealing with any intellectual property that might arise during the research
5. Emergency Disclosure Provisions: Procedures for breaking confidentiality in case of emergencies or legal requirements
6. Digital Data Handling: Specific provisions for handling digital or electronic confidential information
7. Recording and Photography: Provisions regarding any audio, video, or photographic recording during research
1. Research Project Description: Detailed description of the research project and its objectives
2. Types of Confidential Information: Comprehensive list of types of confidential information that will be shared
3. Data Handling Procedures: Specific procedures for handling, storing, and destroying confidential information
4. Contact Information: List of key contacts including research supervisor, data protection officer, and ethics committee
5. Consent Form: Separate but related consent form for research participation
6. Data Privacy Notice: Detailed notice complying with DPA requirements regarding data collection and processing
Authors
Confidential Information
Research Project
Research Institution
Research Participant
Personal Data
Sensitive Personal Information
Principal Investigator
Research Team
Study Materials
Research Data
Permitted Purpose
Unauthorized Disclosure
Data Processing
Research Protocol
Consent
Ethics Committee
Intellectual Property Rights
Research Results
Breach of Confidentiality
Data Subject Rights
Research Records
Authorized Personnel
Confidential Materials
Data Protection Officer
Research Site
Study Period
Third Party
Disclosure
Research Ethics Guidelines
Data Protection
Use Restrictions
Information Security
Return of Materials
Term and Termination
Breach and Remedies
Permitted Disclosures
Regulatory Compliance
Participant Rights
Ethics and Compliance
Duration of Obligations
Intellectual Property
Representations and Warranties
Governing Law
Dispute Resolution
Severability
Force Majeure
Amendment and Modification
Entire Agreement
Notice Requirements
Emergency Disclosure
Survival
Assignment
Third Party Rights
Academic Research
Healthcare
Social Sciences
Scientific Research
Medical Research
Educational Institutions
Pharmaceutical
Technology Research
Psychology
Market Research
Clinical Trials
Biotechnology
Research Operations
Legal
Compliance
Data Protection
Research Ethics
Clinical Operations
Research Administration
Human Subjects Protection
Regulatory Affairs
Research Governance
Research Director
Principal Investigator
Research Coordinator
Ethics Committee Member
Data Protection Officer
Research Administrator
Legal Counsel
Compliance Officer
Research Project Manager
Human Subjects Protection Officer
Research Ethics Administrator
Clinical Trial Manager
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