Anissah Appadu has a diverse work experience in the pharmaceutical and education sectors. Anissah started their career as a Trainee Clinical Trial Coordinator at CIDP - Centre International de Développement Pharmaceutique in May 2016 and later became a Clinical Trial Coordinator, Pharmacovigilance Officer, and Regulatory Affairs Representative. In September 2018, they transitioned to the role of a Clinical Trial Manager while also being responsible for regulatory affairs and pharmacovigilance. Anissah then served as an Operations Planning Lead and Regulatory Affairs Representative before taking on their most recent position as the Head of Projects and Regulatory Affairs Manager. In addition to their experience in the pharmaceutical field, they also worked as an Educator at Imperial College Curepipe from 2015 to 2016. Earlier in their career, Anissah was a Laboratory Technician at SGS from July 2012 to October 2013.
Anissah Appadu pursued their higher education in the field of biology. Anissah started their academic journey in 2008 at Queen Mary University of London, where they completed their Bachelor of Science (BSc) degree in Biochemistry in 2011. After their undergraduate studies, they furthered their education at the University of Mauritius, where they obtained a Master of Science (MSc) degree in Cell/Cellular and Molecular Biology from 2013 to 2015.
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CIDP - Centre International de Développement Pharmaceutique
CIDP, Naturally Innovative Established in 2004, CIDP is a private and independent Contract Research Organisation (CRO) that carries out high-performance R&D activities. With over 17 years of experience in the clinical research, CIDP has a strong foothold on each continent with centres located in Brazil, India, Mauritius, and Romania offering an ideal platform for all your research projects worldwide. The services provided by CIDP are segmented into five main areas of expertise: Research & Development activities, Preclinical in vitro testing, Clinical research, Biostatistics and Data Management and Regulatory Affairs. CIDP comprises a team of 130 staff members: doctors, pharmacists, project managers, clinical research assistant, biostatisticians, biologists, chemists, data managers... and has built over the years an international network of investigators who are highly qualified in their different therapeutic fields. We also have developed an independent Global Quality Assurance department which monitors our studies worldwide. All of our subsidiaries are ISO 9001 certified. The modern and secured offices and the equipment reflect the high quality standard required for the successful conduct of clinical studies. Through its R&I cluster, the centre in Mauritius focuses its investigation on plants and their potential applications in the field of cosmetic, nutrition and therapy. Its geographical position at the heart of the Mascarenes Islands and proximity to the African continent gives it very enviable access to a rich and unexploited flora. From this unique biodiversity and CIDP’s cutting edge expertise in ethno-pharmacology and research, it aims to become a premium provider of novel phytochemicals, proprietary-based ingredient technologies and seamless contract research services on natural products.