We work with a purpose-fit, scalable model, combining in-house experts with trusted collaborators across GMP, clinical development, and regulatory strategy. Here's our core team, with more specialist profiles to be introduced soon.
Jaydon Inott
Founder and Director
Jaydon brings over 20 years of experience at the intersection of clinical development and GMP implementation. He has led end-to end clinical research, launched multiple ventures in cannabinoid and botanical medicines, across UK GMP sites. With a focus on operational rigour and strategic foresight, Jaydon supports clients to build compliant, scalable systems that enable real-world impact. He is an eligible MHRA Quality Controller, RP, and IRCA Lead GMP Auditor.
Edward Fisher
Director- Commercial, Clinical Strategy & Technology Enablement
Edward brings over 20 years of experience in scaling startups and building digital products across health, biotech, and SaaS. He has held commercial and strategic roles in the medicinal cannabis sector and has co-founded multiple ventures, including three CQC-approved clinics. With expertise spanning tech strategy, product development, and go-to-market execution, Edward supports FINA's clients in bridging operational execution with scalable growth offering deep commercial input for clients. He has also played key roles in capital raises, acquisitions, and pharmaceutical distribution.
Kevin Perera
Quality Consultant
Kevin has over 20 years of pharmaceutical experience in a GMP environment across development, manufacturing, quality and validation. Bringing deep, practical expertise to GMP implementation and inspection readiness for botanical and pharmaceutical ventures.
Priyanka Kaushik
Quality Consultant
Quality systems specialist with 6+ years in biopharma, supporting computerised system validation and QMS operations across USFDA and EMA frameworks. Focused on driving compliance, documentation, excellence, and continuous improvement in regulated digital environments.
Mikayla Clark
Business Administrator
Business Administrator with a background in education and psychology. Mikayla supports operational delivery and team coordination across FINA's client projects. She brings strong communication, organisational, and people-focused skills to our fast-pased, regulated environment.
Driving Progress in Medicinal
Cannabis & Phytopharmaceuticals
Compliance isn’t the only goal — traction is. We build lean systems that scale.
Systems That Enable, Not Just Protect
Quality as Your Growth Platform
Quality That Scales With You
Quality is the Engine Room for Innovation
Compliance isn’t the only goal — traction is. We build lean systems that scale.
Driving Progress in Medicinal
Cannabis & Phytopharmaceuticals
Compliance isn’t the only goal — traction is. We build lean systems that scale.
About Fina
FINA is a specialist consultancy supporting ventures in medicinal cannabis, botanical medicines, and herbal pharmaceuticals. We help founders and teams move from vision to validation through regulatory strategy, GMP implementation, and clinical development services.
With deep, cross-disciplinary expertise and a commitment to execution that holds up under scrutiny, we build lean, scalable quality management systems that unlock market access, licensing success, and real-world impact.
FINA Consulting draws on over two decades of cross-disciplinary experience spanning GMP implementation, clinical development, and pharmaceutical licensing. Alongside a growing team of technical specialists, operational leads, and quality professionals, we bring technical expertise grounded in operational experience, commercial acumen and extensive experience in pharmaceutical start-up ventures. We have a track record of delivering clear, cost-sensitive, and scalable strategies to medicinal cannabis ventures, drawing on our own experience and that of our valued clients, always guided by the same ethos: regulatory intelligence is key to market access and long-term success.
Our Services
Clinical Development
· CTA & IMPD Strategy
· Investor-Grade Trial Planning
· Data Positioning & Regulatory Submissions
· Phase II Ready Design & Advisory
GMP Implementation & Inspection Readiness
· Full Site Setup (EU GMP)
· QMS Design & Deployment
· Quality Team Build-Out & Interim QA Roles
· Project Management for Facility
Commissioning
GxP Auditing
· IRCA-Certified GMP Auditors
· Internal Audit Readiness & Supplier Qualification
· Remote & On-Site Audit Packages
Clinic and Pharmacy Integration
· Full-Service Clinic Setup & Licensing
· Pharmacy Operations and Systems
· Enabling vertical integration with joined-Up Solutions from Manufacturer to Dispensing
Latest Blogs
Maria Saraha
Founder
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David Marsh
Co-Founder
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Peter Warner
Co-Founder
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Williams
Co-Founder
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Our Team
Our Core Values
Purpose & Impact
Values that guide our contribution to clients, the sector, and society.
Mindset & Execution
How we approach our own work Principles behind our habits, decisions, and problem-solving.
Team Culture & Collaboration
How we approach our own work
Agreements that shape trust, communication, and shared success.
External Impact & Contribution
What we contribute beyond the project Commitments that shape our role in industry evolution, environmental responsibility, and regulatory progress.