Consent Policy

Our Commitment to Informed Consent

At Savin Medical Group, we believe that informed consent is fundamental to ethical clinical research. We are committed to ensuring that every research participant fully understands the nature, risks, and benefits of any study before agreeing to participate.

Elements of Informed Consent

Before enrolling in any study, participants will receive clear information about:

• The purpose and objectives of the research study
• Expected duration and procedures involved
• Potential risks and discomforts
• Potential benefits to participants or others
• Alternative treatments or procedures available
• Confidentiality protections for personal information
• Compensation and costs, if any
• Contact information for questions or concerns

The Consent Process

Our consent process includes:

1. 1. Document Review: Participants receive written consent documents to review at their own pace.
2. 2. Discussion: Research staff explain the study in detail and answer all questions.
3. 3. Comprehension Check: We verify that participants understand key aspects of the study.
4. 4. Voluntary Decision: Participants are given time to make a voluntary decision without pressure.
5. 5. Documentation: Written consent is obtained and participants receive a copy.

Your Right to Withdraw

Participation in research is always voluntary. You have the right to withdraw from any study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled. Your decision to withdraw will not affect your relationship with Savin Medical Group or your access to standard medical care.

Special Populations

We have additional protections for vulnerable populations, including children, pregnant women, prisoners, and individuals with diminished capacity. These studies require additional safeguards and may involve legally authorized representatives in the consent process.

IRB Oversight

All research conducted at Savin Medical Group is reviewed and approved by an Institutional Review Board (IRB), an independent committee that ensures research is conducted ethically and that participants' rights are protected.