Scientific R&D, custom nutraceutical formulations, lab prototyping, and global compliance for high-performing health brands.
ProTech Health Sciences is a premier OEM supplement formulation and product development partner serving health brands across 40+ countries. Backed by over two decades of technical expertise, our team of formulation scientists and food technologists bridges the gap between raw scientific research and commercial nutraceutical success.
Whether you are seeking custom formulation from scratch, bio-availability optimization, or reformulating an existing supplement to meet stringent international compliance (US FDA, EU EFSA, NPRA, Halal), we deliver rapid prototyping and stability-tested products engineered for market differentiation.
A comprehensive R&D framework designed to minimize market risk, maximize product efficacy, and accelerate commercial rollout.
Bespoke blend creation incorporating clinically studied active ingredients, botanical extract standardization, synergistic micronutrients, and targeted efficacy profiles.
Pre-formulation audit against NPRA, US FDA, EU regulations, and Halal standards to prevent ingredient bans, unauthorized claims, or registration delays in export markets.
Transparent active ingredient cost analysis, yield optimization, and batch size scalability ensuring competitive margin targets without compromising biological efficacy.
Physical sample prototyping with organoleptic testing (flavoring, solubility, mouthfeel) paired with accelerated temperature and shelf-life stability verification.
From initial brief to commercial mass production, our rigorous R&D process ensures consistent batch quality and rapid turnaround.
We review your brand positioning, target demographics, desired health benefit claims, price point goals, and delivery format preferences.
Our formulation scientists select standardized ingredients, determine precise dosing for clinical efficacy, and optimize ingredient synergy.
Bench-top sample production for sensory evaluation, solubility testing, flavor profiling, and physical stability assessment.
Full compliance review of master formula, ingredient origin safety, heavy metal standards, and product claim verification for target countries.
Formula transfer to automated high-capacity GMP lines for commercial scale production, complete with Certificate of Analysis (COA) for every batch.
Our pharmaceutical-grade facilities operate under international quality systems to facilitate seamless global export.
Expert insights into our OEM supplement development, R&D timelines, and custom formulation capabilities.
