Solviva is a reliable partner for international companies in their search for new opportunities by granting manufacturing rights under license or partnering for the marketing and distribution of their products in MENA region. The pharmaceutical manufacturing activities carried to Solviva cover the manufacturing and packaging of non-sterile oral and topical dosage forms: liquids, tablets, capsules, suppositories. Solviva maintains a quality system that ensures consistency in product quality by applying cGMP (Good Manufacturing Practices), GSDP (Good Storage and Distribution Practices), and GLP (Good Laboratory Practices), and complies with local and regional health authorities, licensors and ISO 9001:2015 requirements. Solviva ensures a rigorous Quality Assurance system throughout the different stages along with implementation of Lean manufacturing concepts for a continual improvement approach in line with the industry’s best practices. The Supply Chain Activities in place ensure the development and implementation of built-in quality and cost-effective planning, purchasing, manufacturing and distribution activities. Solviva Manufacturing facility and related premises are periodically audited by licensors and by the health authorities. We are dealing with different manufacturing sites: Greece – Spain – Germany - Netherland -Turkey – Egypt