At Oraxon Bio Pharma, Quality Assurance and Control are paramount. We adhere to rigorous procedures to ensure our manufactured products consistently meet or exceed defined quality criteria, client specifications, and international quality standards.

Our commitment to quality is underpinned by a robust set of predefined standards for both our products and services. These standards are clearly outlined in our Standard Operating Procedures (SOPs). To continually improve, we collect and analyze real-world data.

Oraxon Bio Pharma is a leading global exporter of high-quality ethical and generic pharmaceuticals. Our state-of-the-art manufacturing facilities adhere to stringent international standards, including WHO-GMP, GLP, and ISO certifications.

We specialize in a diverse range of dosage forms across various therapeutic categories, including tablets, capsules, sachets, syrups, nutritional supplements, herbal supplements, and cosmetics. Our dedicated formulation development and regulatory teams continuously strive to bring the latest molecules and innovative formulations to market.

Oraxon Bio Pharma currently exports its products to numerous countries worldwide, with a strong focus on African and South-East Asian markets.

Oraxon Bio Pharma operates a state-of-the-art manufacturing facility in India equipped with advanced infrastructure, including a dedicated transformer-power-station, a closed-loop water treatment system, modern plant and machinery, advanced air-handling units, and an efficient effluent treatment plant.

Our facility is staffed with highly qualified, experienced, and trained personnel specializing in the production of antibiotic dosages. Manufacturing processes adhere strictly to Good Manufacturing Practices (GMP) and revised Schedule-M guidelines. All equipment is properly designed, installed, validated, and maintained, with operations and cleaning procedures strictly adhering to Standard Operating Procedures (SOPs).

We prioritize quality assurance through rigorous process and utility validations, stringent sanitation protocols, and meticulous equipment maintenance. All activities are performed under the supervision of competent personnel, with comprehensive records maintained throughout the production process. Stability studies are conducted in accordance with WHO guidelines.

The facility incorporates robust measures to prevent cross-contamination, ensuring the highest standards of product quality and safety.