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Courses/Law/Substance Abuse

Red Flags & Grey Areas in Psychedelic Practice

Key Considerations for Attorneys in the Psychedelic Space

Created byCLE Companion
4.5
(2 reviews)
BeginnerUpdated May 25, 2024
Red Flags & Grey Areas in Psychedelic Practice

What You'll Learn

check_circleIdentifying High-Risk and Gray Area Clients
check_circleAssessing Substance Legality and Source
check_circleEnsuring Ethical Facilitation and Training
check_circleStructuring Safe and Therapeutic Events

About This Course

This session will illuminate the top 10 issues that attorneys should consider when counseling clients in the psychedelic space. We will address legal concerns, ethical considerations, and best practices on how to build, structure and document your client's psychedelic practice. Attorneys who are aware of these issues will help contribute to a healthy, responsible, and compassionate psychedelic industry.

Course Outline

1. Identifying High Risk and Gray Area Clients2. Substances: source and legality3. Substances: training and ethics of guiding4. Structure of Events5. Intake Documents6. Liability waivers7. Preparation8. Integration

9. Brain Chemistry10. Balancing legal language and compassionate 

 

Your Instructors

CLE Companion
CLE Companion

The Smart Route to CLE Compliance

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CLE Companion is a leading virtual Continuing Legal Education provider offering top-quality courses to lawyers across the US and Canada. Its mission is to utilize technologies to support the completion of CLE with unparalleled convenience and value.    

Barine Majewska
Barine Majewska

Counsel

BARINE MAJEWSKA is counsel in Vicente Sederberg's Denver office, where she is a leading member of the firm's Entheogens and Emerging Therapies Practice Group. She became an attorney because she loved the logical reasoning skills required by law, and grew to enjoy applying those skills to help people and companies be successful in business. After graduating from the University of Virginia School of Law, she joined the corporate department at Cooley LLP, where she worked with technology and startup companies doing venture capital, M&A, and technology licensing work. Later in her legal career, she developed a long-standing respect for psychedelics and plant medicine, which led her to consider going back to school for a PhD in clinical psychology to work in a clinical setting. She was offered a fantastic opportunity to intern in pilocybin studies at the Johns Hopkins School of Medicine, where her firsthand experience working as both a research assistant and guide in psilocybin sessions gave her clear insights into the potency, benefits, and pitfalls of psychedelic work. In 2016, Barine returned to law and joined VS. She was recently appointed to a leadership role in VS’s Enthogens and Emerging Therapies Practice Group. In this role, Barine applies VS’s pioneering spirit in the cannabis industry to fostering the effective, safe, and legal use of psilocybin, ketamine, MDMA, and other entheogens. She is fascinated by the ethical, cultural, spiritual, psychological, and commercial challenges and opportunities presented by this emerging industry. In addition to her work in the psychedelic space, she assists clients with corporate and intellectual property licensing matters, and loves working with driven, innovative clients. She has deep interests in meditation, biohacking, and the many types of altered states of consciousness accessed throughout human history via different technologies. She holds an undergraduate degree in physics, and is fluent in Turkish.

Credit Information

What Students Are Saying

4.5
Student's Choice
2 reviews

Frequently Asked Questions

We are a registered provider with 327+ associations and regulatory bodies worldwide. We operate across 29 global markets including Canada, the US, Australia, and the UK. Every course page clearly displays its specific accreditations. Upon completion, you receive a professional certificate that can be validated online. Our certificates include all necessary accreditation details, credit hours, and completion dates, and are formatted specifically to meet the submission requirements of most global regulatory bodies.