Henrietta Udoruisi is a seasoned pharmaceutical and analytical chemistry professional with extensive experience in the quality-control testing of raw materials used in medicinal drugs, food products, and cosmetics. She plays a critical role in ensuring that all ingredients and active substances meet stringent regulatory and safety standards before reaching the public.
Her current work focuses on the chemical analysis of pharmaceutical excipients and APIs, applying advanced instrumentation and chromatographic techniques to detect impurities and toxic levels of compounds. Henrietta also oversees supplier audits, conducting extended analytical evaluations to verify material integrity and traceability across global supply chains.
Having previously worked with leading pharmaceutical companies such as GlaxoSmithKline and Roche, she brings a wealth of experience in GMP-compliant laboratory practice, pharmaceutical regulatory compliance, and method validation. Her passion lies in protecting public health by advancing transparency, safety, and quality in every stage of product development.
Henrietta continues to contribute to the intersection of science and safety—ensuring that medicines, foods, and beauty products remain safe, effective, and beneficial for every consumer.
Ensuring the quality, identity, and purity of raw materials and finished pharmaceutical products through advanced analytical methods including HPLC, GC-MS, UV-Vis, and spectroscopy.
Performing comprehensive audits and material verifications to maintain compliance with FDA, EMA, and WHO GMP standards across pharmaceutical, food, and cosmetic sectors.
Promoting transparency in the global ingredient supply chain and advancing safe formulations that minimize exposure to potentially harmful chemical agents.
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