About TEDDZ Regulatory Affairs
We are your dedicated regulatory partners, committed to guiding your product from strategy to submission and beyond.
Our Mission: Your Expertise-Led Regulatory Partner
In the complex, high-stakes world of pharmaceutical and healthcare products regulation, agility and senior expertise are what make the difference. TEDDZ Regulatory was founded to provide a new kind of regulatory partnership: one that embeds directly with your team, offering the high-touch service of an in-house expert with the breadth of a global consultant. We exist to make your regulatory journey clear, compliant, and successful.
Meet Our Leadership
Timi Adetona
Founder & Principal Regulatory Consultant
With over 25 years of hands-on experience in regulatory affairs, Timi has led complex submissions for both innovative biotech startups and global pharmaceutical assets, including those for rare diseases. Timi founded TEDDZ Regulatory with a passion for navigating the specific challenges and nuances of the MHRA, EMA, and key African agency frameworks. My focus is on providing pragmatic, strategic regulatory advice and operations that gets products to patients efficiently.
The TEDDZ Difference
Agile,
Embedded
We act as a seamless extension of your team, adapting to your timelines and providing support across all global time zones.
Senior Expertise, Always
When you partner with TEDDZ, you get senior-level attention. We don’t delegate your high-stakes projects to junior staff.
Specialist Geographic Focus
We provide deep, practical expertise in our core markets: the UK (MHRA), EU (EMA), and key African agencies (NAFDAC, SAHPRA).
Let’s Do It Together
Let’s Discuss Your Project
Ready to partner with an expert team that will guide your regulatory journey? Book your free 30-minute consultation.