Enigma Biosciences was founded on a single conviction: that the highest standards of pharmaceutical manufacturing should be accessible to every innovator — not just the largest corporations.
The principles that guide every decision, every batch, and every client relationship.
We hold every batch to the same standard regardless of client size or order volume. A 500-unit pilot run receives the same QC scrutiny as a 500,000-unit commercial order.
We invest in R&D to stay at the frontier of formulation science — from next-generation nano delivery systems to novel excipient combinations — so our clients bring better products to market faster.
We assign a dedicated formulation scientist, QA lead, and project manager to every engagement. Your success is our success — measured in products that reach market and stay there.
Digital batch records, real-time production status, and complete documentation are available through your client portal at any time. No black boxes — you see exactly what we see.
We never cut corners on compliance. Our regulatory team stays ahead of FDA, EU, and international guidance — so your products are submission-ready from day one.
We build processes that scale from bench to commercial from the start. Our pilot-to-production methodology means zero reformulation surprises when you're ready to grow.
Decades of combined expertise across pharmaceutical development, regulatory affairs, and precision manufacturing.
A seasoned entrepreneur and C-suite executive, Mr. Williams has a demonstrated track record of starting and managing high growth companies.
Specializes in nanoemulsion and liposomal drug delivery. PhD in Thermal Dynamics; seasoned electrical and thermal dynamics engineer specializing in supercritical systems for industry applications.
Serial entrepreneur with 35 years building brands and companies in Consumer Products, OTC Drug, Cosmetic, Nutritional Supplements, and Agriculture/Remediation market segments.
Our 30,000 sq ft Orlando facility houses five dedicated manufacturing lines, an in-house analytical lab, and a controlled R&D suite — all operating under a single unified quality management system.
The facility is FDA-registered and inspected, GMP-certified, and built to ISO cleanroom standards for critical manufacturing zones. We welcome client audits at any time.
Tell us about your formulation challenge. Our scientists will review your requirements and come back with a tailored manufacturing brief — no commitment required.
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