Dr. Divine Akumo

Contribute in writing; - Clinical Study Protocol and Report (CSP & CSR) - Writing patients narratives - Patient information and informed consent - IBs and CTDs - Technical document management - Compilation of PBRERs/ PSURs and RMPs in accordance to relevant EMA and FDA guidance

- Monitoring of clinical trial phase I – IV studies, non-interventional studies, medical device studies according to international and national regulations - Guarantee that Clinical trial is conducted in accordance to protocol, ICH-GCP and applicable regulatory requirements - Compiling essential documents from site applicable for submission and TMF

Establishment of SHA technique for the detection, identification and quantification of rRNA gene in E. coli.

Exploiting in-vitro cell culture techniques for the extraction of plants bioactive secondary metabolites

Identification of QTL influencing quantitative traits / diseases using mouse model and pig - gene sequencing

- General pharmacology and pharmacokinetics - ICH-GCP - Clinical trial logistics - Monitoring - Data management - Computer application for clinical research - Business and legal English for the bio-pharmaceutical industry - Communication and presentation skills

Identification of genomic variants influencing litter size in pigs

Identification of DNA loci influencing litter size heterosis in mice

- Biochemistry, microbiology and medical laboratory technology - Clinical Biochemistry