We manufacture your supplements to global standards — formula to shelf

MOQ varies by dosage form, packaging and ingredients. Send us your product details and we will come back with the minimum quantity and pricing for your specific case.

Delivery typically runs 45 to 90 days from formula sign-off and arrival of packaging materials. The exact figure depends on raw-material availability, formula complexity and batch size, and we set a clear schedule with every quotation. Candidly: demand sometimes runs ahead of our capacity, which can extend that window — we would rather say so upfront than commit to a date we cannot hold. Regulatory registration runs in parallel and has its own timeline, largely outside our control.

Yes. Our R&D team can build a new formula from your brief, or adapt an existing one to suit your market or regulatory requirements. We have developed more than 1,500 formulas and products to date.

We provide the manufacturing and quality documentation needed for a registration dossier. Registration procedures themselves differ by market — tell us your target market and we will walk through the steps.

Yes, we produce samples for evaluation before commercial production begins. Terms depend on the product and formula.

Yes — that is the core of our business. We manufacture entirely under your brand (private label / OEM) and have produced more than 1,500 formulas and products for over 500 companies to date. Egyptian law requires the manufacturer name on the pack, so Organix appears alongside your brand as a quality signal.

Our facility in Sadat City produces up to 3 million units per month across all dosage forms combined — tablets, capsules, sachets, jars, bottles and liquids.

We have exported to eleven markets: Saudi Arabia, the United Arab Emirates, Iraq, Jordan, Libya, Yemen, Turkey, China, Sierra Leone, Niger and Togo — covering the Gulf, the Levant, North and West Africa, and Asia.

Seven: ISO 9001:2018 for quality management, ISO 22000:2018 for food safety, ISO 45001:2018 for occupational health and safety, FSSC 22000, GMP, the Egyptian NFSA White List, and the Egypt Seal of Quality. Production areas meet Class D clean room requirements.

Thirteen: tablets, bi-layer tablets, effervescent tablets, hard gelatin capsules, powder sachets, effervescent powder sachets, powder jars, powder bags, liquid sachets, semisolid sachets, drops and syrups, semisolid jars, and bottles. The effervescent department (tablets and powder) is our newest production line.

Yes. Organix is registered with the Saudi Food and Drug Authority (SFDA) and is an approved exporter with Egypt's Food Export Council, alongside our NFSA White List listing at home.