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Assent Consent Form Template for Singapore

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Key Requirements PROMPT example:

Assent Consent Form

"I need an Assent Consent Form for a medical research study at Singapore General Hospital, involving collection of blood samples from adult participants, with specific provisions for data sharing with international research partners."

Document background
The Assent Consent Form is a critical document used in Singapore to ensure ethical and legal compliance when obtaining consent from individuals. It is required whenever organizations conduct research, perform medical procedures, or collect personal data that requires explicit consent. The form must comply with Singapore's PDPA 2012, Healthcare Services Act 2020, and other relevant regulations. It typically includes detailed information about the purpose of consent, risks and benefits, participant rights, and withdrawal procedures. The document is particularly important in protecting vulnerable populations and ensuring informed decision-making.
Suggested Sections

1. Title and Date: Clear identification of the document and date of execution

2. Participant Information: Details of the person giving consent including full name, identification number, and contact information

3. Purpose and Scope: Clear explanation of what the consent is for and its scope

4. Rights and Obligations: Description of participant's rights and any obligations

5. Declaration of Consent: Explicit statement of consent and understanding

6. Signature Block: Space for signatures, dates, and witness information

Optional Sections

1. Parental/Guardian Consent: Additional section required when participant is a minor or lacks capacity to provide consent

2. Withdrawal Procedures: Section detailing the process for withdrawing consent, typically included for ongoing studies or long-term consent arrangements

3. Risks and Benefits: Section explaining potential risks and benefits, particularly important for medical procedures or research participation

Suggested Schedules

1. Information Sheet: Detailed information about the procedure/research/purpose requiring consent

2. Contact Information Schedule: List of relevant contact persons and emergency contacts

3. Terms and Conditions: Detailed terms and conditions applicable to the consent being given

Authors

Alex Denne

Head of Growth (Open Source Law) @ ¶¶Òõ¶ÌÊÓÆµ | 3 x UCL-Certified in Contract Law & Drafting | 4+ Years Managing 1M+ Legal Documents | Serial Founder & Legal AI Author

Relevant legal definitions



























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Industries

Personal Data Protection Act 2012: Singapore's primary data protection legislation that governs the collection, use, and disclosure of personal data, including requirements for valid consent and individual rights regarding their personal data

Human Biomedical Research Act 2015: Regulates human biomedical research in Singapore, including requirements for informed consent in medical research contexts

Healthcare Services Act 2020: Provides framework for healthcare services regulation in Singapore, including aspects of patient consent and information handling

Mental Capacity Act: Governs decision-making on behalf of persons lacking mental capacity, including provisions for consent in such situations

Age of Majority Act: Defines the legal age of majority in Singapore and impacts consent requirements for different age groups

Children and Young Persons Act: Contains special provisions for consent from minors and requirements for parental/guardian consent

Electronic Transactions Act: Governs the validity of electronic signatures and electronic documents in Singapore, relevant for digital consent forms

Contract Law of Singapore: Provides fundamental principles for valid consent, including capacity to consent and clear communication requirements in contractual agreements

IRB Guidelines: Institutional Review Board guidelines that govern research involving human subjects and consent requirements in research contexts

Singapore Good Clinical Practice Guidelines: Standards for conducting clinical research in Singapore, including specific requirements for informed consent in clinical trials

Bioethics Advisory Committee Guidelines: Provides ethical guidelines and recommendations for consent in biomedical research and healthcare contexts

Teams

Employer, Employee, Start Date, Job Title, Department, Location, Probationary Period, Notice Period, Salary, Overtime, Vacation Pay, Statutory Holidays, Benefits, Bonus, Expenses, Working Hours, Rest Breaks,  Leaves of Absence, Confidentiality, Intellectual Property, Non-Solicitation, Non-Competition, Code of Conduct, Termination,  Severance Pay, Governing Law, Entire Agreemen

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