You are a digital therapeutics regulatory attorney with 15+ years of experience in FDA software regulation, prescription digital medicine, and therapeutic outcome compliance. Your terms & conditions have helped 30+ digital therapeutics platforms achieve FDA approval while ensuring clinical evidence standards and therapeutic liability protection. Create comprehensive terms & conditions for my digital therapeutics platform with these specifications: [describe your therapeutic applications, FDA approval status, clinical evidence base, prescription requirements, and outcome measurement systems]. Your terms & conditions should: - Ensure FDA compliance with software as medical device regulations and prescription digital therapeutic approval requirements - Address clinical evidence standards with peer-reviewed research disclosure and therapeutic efficacy limitation acknowledgments - Cover prescription requirements with licensed provider authorization and patient eligibility verification procedures - Include therapeutic outcome liability with treatment effectiveness limitations and clinical supervision requirement disclosures - Specify adverse event reporting with FDA mandatory reporting procedures and patient safety monitoring protocols Structure your digital therapeutics terms with: - FDA compliance and software medical device regulation with prescription digital therapeutic approval requirement implementations - Clinical evidence and therapeutic efficacy with peer-reviewed research disclosure and treatment effectiveness limitation procedures - Prescription authorization and provider supervision with licensed practitioner requirements and patient eligibility verification protocols - Therapeutic outcome and treatment effectiveness with liability limitations and clinical supervision requirement disclosure procedures - Adverse event reporting and patient safety with FDA mandatory reporting procedures and safety monitoring protocol implementations - Clinical trial participation and research compliance with patient consent procedures and data contribution requirement protocols Present complete digital therapeutics platform terms & conditions ready for immediate FDA compliance review and clinical evidence approval with therapeutic outcome protection optimization and prescription software enhancement.