Informed Consent for Stem Cell Therapy

At Viezec, we believe that informed consent is a fundamental part of ethical, patient-centered medical care. Before undergoing any stem cell-based regenerative treatment, every patient has the right to fully understand the proposed therapy, its potential benefits, possible risks, available alternatives, and expected outcomes.

Informed consent is not just a form. It is an ongoing communication process between you and our medical team. Our goal is to ensure that you feel confident, informed, and empowered to make decisions about your health.

Informed consent is a medical and ethical process that ensures you receive clear, accurate, and complete information about a treatment before agreeing to proceed. This includes:

• The nature and purpose of the proposed treatment

• Potential benefits and realistic expectations

• Known and possible risks or side effects

• Alternative treatment options

• The option to decline or postpone treatment

• The opportunity to ask questions and receive understandable answers

This process supports patient autonomy and protects your right to make voluntary, well-informed healthcare decisions.

Stem cell therapy is an advanced field of regenerative medicine that aims to support the body’s natural repair and healing processes. Depending on the protocol, stem cells or cell-based products may be used to help manage certain degenerative, inflammatory, or injury-related conditions.

It is important to understand that:

• Stem cell therapy is not a guaranteed cure

• Results can vary between individuals

• Some applications are still considered investigational or emerging

• Scientific evidence continues to evolve

Your care team will explain the specific type of therapy proposed for your condition, including the source of cells, processing methods, and treatment goals.

Depending on your medical condition, potential benefits may include:

• Reduction in pain or inflammation

• Improvement in function or mobility

• Support for tissue repair processes

• Enhancement of quality of life

However, outcomes are individualized. No ethical medical provider can guarantee specific results.

As with any medical procedure, stem cell therapy may carry risks. These may include, but are not limited to:

• Infection at the injection or infusion site

• Pain, swelling, or localized inflammation

• Allergic or immune reactions

• Lack of clinical improvement

• Rare but serious complications depending on treatment type

Some risks may not be fully known due to the evolving nature of regenerative medicine. These risks will be discussed in detail before treatment.

You have the right to know about reasonable alternative treatments, which may include:

• Conventional medical or surgical treatments

• Physical therapy or rehabilitation

• Medication-based management

• Watchful waiting or conservative care

Your physician will discuss whether alternative options may be appropriate for your specific condition.

Participation in any treatment at Viezec is entirely voluntary. You have the right to:

• Decline treatment

• Delay your decision

• Withdraw consent at any time before treatment

• Seek a second medical opinion

Your decision will be respected without pressure or obligation.

All regenerative and stem cell–based treatments at Viezec are conducted under the supervision of qualified medical professionals. Each patient’s treatment plan is developed based on individual medical history, diagnostic findings, and clinical assessment.

The treatment process may involve medical evaluation, laboratory review, imaging review where applicable, and determination of treatment suitability. Clinical protocols are followed to promote patient safety, proper handling of biological materials, and appropriate administration techniques.

Patients are informed about the general steps involved in their treatment process and what to expect before, during, and after the procedure. This ensures transparency and helps patients feel prepared for their care experience.

We encourage you to actively participate in the consent process. You are encouraged to:

• Ask questions

• Request clarification of medical terms

• Take time to review written consent materials

• Discuss concerns with your family or advisors

Our medical team is committed to ensuring you understand the information provided.

Once all information has been reviewed and your questions have been addressed, you may be asked to sign a written informed consent form. This document confirms that:

• You received adequate information

• You understand the potential benefits and risks

• You had the opportunity to ask questions

• You voluntarily agree to proceed

Viezec follows ethical medical practices and emphasizes transparency, patient safety, and responsible care. Stem cell and regenerative therapies are subject to varying regulations depending on jurisdiction and treatment type.

We are committed to:

• Ethical sourcing and handling of biological materials

• Compliance with applicable medical standards

• Honest communication about limitations and uncertainties

• Avoidance of exaggerated claims or guaranteed outcomes

We believe the best outcomes occur when patients and providers work together. Informed consent at Viezec is part of a shared decision-making model that respects your values, goals, and medical needs.

Our priority is your safety, understanding, and trust.

Not all patients are suitable candidates for regenerative or stem cell–based therapies. Medical suitability is determined through review of medical records, current health status, and the nature of the condition being treated.

Certain medical conditions, active infections, uncontrolled chronic illnesses, or other risk factors may affect eligibility. In some cases, patients may be advised to postpone treatment or pursue alternative care options.

Viezec reserves the right to determine whether a patient is an appropriate candidate for a proposed therapy based on clinical judgment and safety considerations. This helps protect patient well-being and ensures responsible use of regenerative treatments.

As part of its commitment to continuous improvement and responsible medical practice, Viezec may collect de-identified clinical data related to treatment outcomes, patient-reported improvements, and safety observations.

This information may be used internally for quality assurance, treatment optimization, and evaluation of clinical protocols. Any such data collection is handled in accordance with applicable privacy and confidentiality standards.

Participation in outcome tracking or internal quality initiatives does not affect a patient’s right to privacy and does not replace formal clinical research unless separately disclosed and consented to.

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