Regulatory Affairs Department is the Channel between EIPICO and Regulatory Bodies, for both Local and International markets.
Regulatory Affairs Department Responsibilities :
It is responsible for the presentation of registration documents to regulatory agencies, carrying out all the subsequent negotiations necessary to obtain New Marketing Authorizations enriching EIPICO's Portfolio, as well as, maintaining marketing authorizations for the 'Already Registered' Products.
EIPICO has 400 product registration files across 65 countries.
On an international level, EIPICO has 82 products presented with the highest level of quality, in CTD format, ready for exportation. We strive to transfer All EIPICO Products into CTD format within 5 years.
Regulatory Affairs Department gives strategic and technical advice to managerial levels, making an important contribution, both scientifically and commercially, to the success of the development program and the company as a whole.
Regulatory Affairs Department is responsible for Trade Marks and Patencies, assuring that all Company rights are preserved.
Find out moreQuality Assurance EIPICO has been accredited ISO Certificates besides Certificates from European, African, and Asian Health Authorities.
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R&D We believe in continuous discovery, improvement and creativity; that’s why we invest annually in our R&D labs to bring the state-of-the-art equipment for the formulation, characterization and analytical activities.
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Quality ControlWe support our incoming raw materials, packaging materials and products with timely and accurate test results, that meet the most recently issued pharmacopoeial references.
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