Biontera connects formulators with liposomal forms and branded active ingredients manufactured evidence-first (with ALCOA+ data integrity) at GMP-certified facilities — including US FDA-approved and US FDA-registered sites. For global ingredient innovators, we are the exclusive, science-literate route into the Turkish market, backed by four decades of pharma industry experience.
Built on more than four decades in the Turkish pharmaceutical sector, Biontera gives international formulators, contract manufacturers and brands a single evidence-first source for clinically supported, patent-driven active ingredients accepted in international markets; ingredients we evaluate on their data, not their marketing.
Read our storyEvery branded ingredient we offer is supported by peer-reviewed bioavailability or efficacy studies; evidence precedes every claim we make.
BioSOLVE®, Aquasol™, Liposomal and Nano-Liposomal systems deliver effective solutions to solubility and absorption challenges.
Our central facility at Başkent OSB operates under Good Distribution Practice (GDP) standards. Smart climate control, +2/+8 °C cold-chain and end-to-end log tracking ensure full ingredient security.
Ingredients are manufactured under GMP at audited facilities (including US FDA-approved and US FDA-registered sites) and arrive with technical files aligned with ALCOA+ data-integrity principles and compliant with Turkish food supplement and pharmaceutical regulations.
Each of our featured branded ingredients holds a distinct indication area and patented technology. The slider below introduces the actives available single-source through Biontera, with the evidence in hand.
Branded active ingredients accessible only through Biontera in Türkiye. Each accelerates product development with proven mechanisms of action, distinctive technologies and published evidence, wherever you formulate.
8.9× higher bioavailability vs. market curcumin; 12-week clinical study in rheumatoid arthritis reporting a −74.96% VAS pain change vs −8.33% under placebo.
Natural ingredient with gastric protective properties. Provides mucosal protection and acid neutralization for gastric-comfort formulations.
Clinically supported natural ingredient for menopausal symptoms and skin vitality. Indispensable for cosmeceutical and women's health formulations.
Clinically validated extract supporting cognitive performance, memory and reaction time. Optimized for esports and cognitive health products.
A registered complex with efficacy demonstrated in 2 separate clinical publications for muscle recovery, endurance and athletic performance.
Clinically validated natural alternative for constipation management without irritation. Published in IJTCM 2022.
High-bioavailability, stable beta-carotene source. Core ingredient of eye health, skin and general antioxidant formulations.
Berberine engineered with BioSOLVE technology. 4× enhanced absorption for glucose- and lipid-metabolism support formulations.
The biologically active form of folate. About 40–60% of the population carries an MTHFR polymorphism that hinders folic acid conversion — L-Methylfolate bypasses this enzyme step entirely.
88× higher bioavailability vs. market vitamin C. Pediatric clinical research data in the upper-respiratory health area.
We provide single-source access in Türkiye to branded active ingredients from leading international manufacturers. For global ingredient innovators, we act as an exclusive, science-literate representative in the Turkish market, a partner that reads the data before making the claim.
Hyderabad / India · Active in 17+ countries
Owner of BioSOLVE® patented technology. A US FDA-registered, GMP and FSSAI certified manufacturer of clinically validated branded botanical ingredients and patented absorption platforms.
Chennai · Padappai (Tamil Nadu) / India · ICH-standard production
A US FDA and Türkiye TİTCK-approved pharmaceutical API manufacturing facility. Operating to WHO-GMP, EU, ICH and USP standards, Molclone Labs is a globally recognized producer of advanced vitamin forms and niche APIs. Biontera holds the exclusive Türkiye distributorship for high-value actives such as Calcium L-5-Methyltetrahydrofolate and Pentosan Polysulfate Sodium.
Aurangabad / India · 26,000 sq.ft. facility
A GMP manufacturer and developer of the Liposomal, Nano-Liposomal and Aquasol™ proprietary platforms. India's first domestic manufacturer of creatine and CoQ10.
India · GRAS & FSSAI approved strains
Our core partner with proprietary probiotic strains for pediatric, women's, renal and cognitive health formulations. Each strain has its own clinical dossier.
Mumbai / India · Since 1993
An SGS GDP certified API supply partner with over three decades of international export experience. Tricon Enterprises supplies Active Pharmaceutical Ingredients across anesthetics, anticoagulants, anti-allergy and niche therapeutic categories — backed by WHO-GMP and DMF documentation — into the Turkish market.
Our active ingredients are produced with four advanced technologies (led by liposomal systems) designed to overcome the bioavailability limitations of traditional forms, with data integrity maintained at every step.
Stable liposomes confirmed by TEM and phase-contrast images that boost bioavailability by orders of magnitude over conventional forms.
A proprietary platform that achieves over 95% water-solubility for fat-soluble actives. Opens the door to functional beverages and liquid dosage forms.
Sub-100 nm particles deliver transdermal permeability and dual water/oil solubility. Ideal for topical nutraceuticals and functional liquids.
A registered formulation technology that optimizes solubility and absorption. The basis of branded curcumin (BioSOLVE Curcumin) and Metaberine products.
Actives in the portfolio are manufactured at GMP-certified facilities — including US FDA-approved and US FDA-registered sites — under ALCOA+ data-integrity systems. Every lot is traceable with its certificate of analysis, stability data and batch records.
Browse the clinical publication archiveMolclone Labs' Chennai plant is approved by the US FDA and TİTCK. Zeus Hygia is US FDA-registered and GMP/FSSAI certified. Facility quality documents are shared on request.
Manufacturing and analytical records are kept to ALCOA+ principles: attributable, legible, contemporaneous, original and accurate.
Every shipment is delivered with a lot-based certificate of analysis (CoA); a 12-item technical dossier is added on request.
The structural integrity of liposomal forms is verified by TEM imaging; bioavailability multiples are documented in peer-reviewed publications.
With active international markets, a portfolio backed by clinical studies and manufacturing partners operating under GMP (including US FDA-approved and FDA-registered sites), we set the standard for branded active ingredients in Türkiye.
Our branded active ingredients are already used safely in countries with the most demanding regulatory environments. That acceptance shortens the path to market for every manufacturer who sources through Biontera.