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English French Portuguese SpanishAgnivesh Health Care Centre (AHCC PVT. LTD.) provides industry-leading custom supplement formulation and R&D services for pharmaceutical, nutraceutical, and wellness brands looking to bring novel, scientifically differentiated products to market. Our team of experienced formulation scientists, pharmacognosists, and regulatory specialists design custom active ingredient blends with verified bioavailability, taste masking, and physical stability. With 20+ years of R&D expertise and 150+ bespoke formulations developed for 120+ active B2B brand partners, we transform complex therapeutic concepts into scalable, commercially viable reality.
Every winning supplement starts with sound biochemical synergy. Our laboratory addresses solubility challenges, prevents ingredient degradation, optimizes delivery vectors, and ensures clean-label status with plant-based excipients. Discover our R&D insights on custom formulation development for nutraceutical capsules.
Combining natural bio-enhancers (e.g. piperine, lipid carriers, liposomes) to maximize cellular uptake of fat-soluble and water-soluble actives.
Environmental chamber stress testing under varied temperature and humidity conditions to guarantee label claim potency across full shelf life.
Your proprietary formulation recipes belong exclusively to you, backed by binding non-disclosure agreements (NDAs) and patentable data packages.
Core therapeutic areas where our R&D formulation laboratory excels:
All custom formulation data is verified with HPLC, FTIR, and microbiological testing protocols to ensure effortless regulatory registration worldwide.
Bridging traditional botanical wisdom with contemporary pharmaceutical chemistry, Agnivesh (AHCC PVT. LTD.) helps visionary supplement brands overcome complex stability hurdles, enhance bioactive efficacy, and achieve true product differentiation.
In-house analytical and pilot formulation laboratories.
Unmatched Ayurvedic standardization combined with modern science.
Formulations built from day one for international regulatory compliance.
Lipid carriers and dual-release technology for enhanced uptake.
Evaluate real physical samples before committing to full production.
Full formulation ownership and confidentiality agreements.
ICH-compliant stability testing under extreme environmental stress.
Seamless process transfer from pilot lab to high-speed factory lines.
Every custom formulation developed in our laboratory is verified against global quality standards. Our facility is registered with the U.S. Food and Drug Administration (USFDA) and operates under a quality management system supported by WHO-GMP, ISO 22000:2018, HALAL, and Organic certifications. Learn more about our quality certifications & compliance standards.
Off-the-shelf supplements compete on price; custom engineered formulations compete on efficacy, novelty, and customer retention. Here is why leading supplement brands formulate with Agnivesh.
Create trademarked formula blends that cannot be replicated or undercut by generic copycat brands.
Scientifically validated delivery mechanisms ensure consumers experience tangible results faster.
Solve active degradation, hygroscopic powder instability, and volatile active oxidation challenges.
Formulate without artificial silicon dioxide, magnesium stearate, titanium dioxide, or harsh binders.
Science-backed unique formulations support higher price points, greater perceived value, and customer loyalty.
Every recipe is accompanied by assay testing protocols, stability data, and claim substantiation dossiers.
A rigorous 6-step laboratory workflow ensuring your custom supplement formulation is safe, stable, and commercially scalable.
Assessing client targets, ingredient therapeutic dosages, and health claim substantiation.
Matching optimal lipid carriers, natural disintegrants, and plant-based capsule shell compatibility.
Producing small benchtop trial batches for sensory, physical, and analytical evaluation.
Thermal and humidity chamber testing to verify zero active degradation over specified shelf-life.
Compiling master formula cards, raw material specs, test methods, and certificate of analysis (CoA).
Transitioning pilot formulation to high-speed commercial production lines with validated parameters.
Collaborate directly with our formulation scientists. Contact our R&D center today to schedule a confidential formulation feasibility consultation.
From concept to delivery
On time, every time
Built on trust and quality
Discover how our formulation R&D team supports you through prototyping, testing, and production scaling. Have general queries? Visit our comprehensive FAQ center.
Get in touch with our formulation experts.
You do! All custom recipes developed specifically for your brand under our R&D agreement are protected under binding NDAs, and full commercial ownership is assigned to your company.
Yes, we frequently reverse-engineer, optimize, and reformulate underperforming products to solve clumping, oxidation, bitter active notes, and shelf-life degradation.
Initial prototype pilot samples are typically delivered in 2 to 3 weeks. Accelerated stability profiling and final formula lock usually take an additional 2 to 4 weeks depending on active complexity.
Our testing suites feature High-Performance Liquid Chromatography (HPLC), FTIR spectrophotometers, dissolution apparatus, moisture analyzers, and environmental stability chambers.
Yes, our formulation specialists specialize in non-GMO, organic, vegan HPMC, allergen-free, and clean-label natural excipient blends without artificial flow agents.
Yes, we manufacture small-batch clinical trial supplies, placebos, and comparative samples with full analytical batch records meeting ethical committee standards.
