The Regulatory Affairs Department at EIPICO serves as the crucial link between the company and regulatory bodies, locally and internationally.
Their responsibilities include preparing registration documents, negotiating marketing authorizations, and maintaining existing product approvals.
With a vast portfolio of 1150 registered products in 67 countries, EIPICO strives to meet global regulatory requirements.
The department provides strategic advice, ensuring compliance with industry standards and protecting the company's intellectual property.
Their expertise and contributions contribute to the overall success of EIPICO's development programs and market presence.
Find out moreGlobal Accreditation EIPICO has been accredited ISO Certificates besides Certificates from European, African, and Asian Health Authorities.
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R&D And Quality 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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