Rameda Pharmaceuticals
Dina Abu Zeid is an experienced professional in the pharmaceuticals and beauty industries, currently serving as the OTC & GIT Senior Product Manager at Rameda Pharmaceuticals since July 2022. Prior to this role, Dina worked as a Brand Manager for the Beauty Category at Vitabiotics Ltd and held positions including Sales and Marketing Manager at ICIM International - BioNike and Brand Manager at Bioderma In Company. Additional roles include Marketing Coordinator and Professional Trainer & Trade Brand Manager at Laboratoires Filorga. Dina began their career as a Medical Sales Representative at Bioderma In Company. Educational qualifications include a Bachelor's degree in Pharmacy and Biotechnology from The German University in Cairo and studies at Islasca.
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Rameda Pharmaceuticals
Our Vision: To become the most valuable emerging pharmaceutical company in Egypt. Our Mission: To provide our customers quality health care solutions in a cost effective manner by developing products and services that satisfy their health requirements. Establishment Rameda began operations in 1994 and was established by a group of Gulf investors with the intention of creating one of the largest pharmaceutical operations in the region. Owners hired V-Konsult of Germany to create a state-of-the art design. Contracted British Carter Construction company to build the Rameda’s facilities. Partnership with Alcon In 1999, Rameda entered into an agreement with Alcon to manufacture – under license - their ophthalmology products. In order to guarantee the quality of their products, Alcon built one of the highest quality eye production facilities in the region at Rameda. Quality enhancement Rameda renewed the syrup production to become GMP (Good Manufacturing Practice). A new Beginning In 2011, Compass Capital led a consortium of private equity investors for the acquisition of 100% of Rameda. Compass Capital plans to establish Rameda as a regional leader in the industry. To execute this strategy Rameda hired a new management team with a proven track record to complement the existing team. Company has commissioned M+W Group to transform solid dosage and beta lactam areas into GMP. Brining entire facility to compliance.