This is my pleasure to recommend Deeksha, who was my student at Crown Medical Research and Pharmaceutical Sciences College of Canada. Under my direct supervision, Deeksha has completed the coursework on Health Canada and ICH-GVP (E2) topics on collecting, assessing, reporting and preventing Safety issue related to the use of medicinal products, Management of safety reporting and submissions to regulatory authorities, Writing safety summary reports in Clinical trials, and Pharmacoepidemiological studies in post marketing phase, and ICSR causality assessments. Deeksha has practical knowledge and experience in clinical trial application, protocol amendments, notification, and submission processes, as well as regulatory compliance. She has experience and knowledge of managing submissions and tracking approvals, reviewing and evaluating adverse event reports, creating and maintaining safety databases, reporting adverse events, managing safety issues, ensuring compliance, developing safety procedures and protocols, and ensuring the safety and efficacy of drugs and medical products. I strongly believe that Deeksha will be an excellent addition to a strong team in the pharmaceutical field.

This is my pleasure to recommend Deeksha, who was my student at Crown Medical Research and Pharmaceutical Sciences College of Canada. Under my direct supervision, Deeksha has completed the coursework on Health Canada and ICH-GVP (E2) topics on collecting, assessing, reporting and preventing Safety issue related to the use of medicinal products, Management of safety reporting and submissions to regulatory authorities, Writing safety summary reports in Clinical trials, and Pharmacoepidemiological studies in post marketing phase, and ICSR causality assessments. Deeksha has practical knowledge and experience in clinical trial application, protocol amendments, notification, and submission processes, as well as regulatory compliance. She has experience and knowledge of managing submissions and tracking approvals, reviewing and evaluating adverse event reports, creating and maintaining safety databases, reporting adverse events, managing safety issues, ensuring compliance, developing safety procedures and protocols, and ensuring the safety and efficacy of drugs and medical products. I strongly believe that Deeksha will be an excellent addition to a strong team in the pharmaceutical field.

This is my pleasure to recommend Deeksha, who was my student at Crown Medical Research and Pharmaceutical Sciences College of Canada. Under my direct supervision, Deeksha has completed the coursework on Health Canada and ICH-GVP (E2) topics on collecting, assessing, reporting and preventing Safety issue related to the use of medicinal products, Management of safety reporting and submissions to regulatory authorities, Writing safety summary reports in Clinical trials, and Pharmacoepidemiological studies in post marketing phase, and ICSR causality assessments. Deeksha has practical knowledge and experience in clinical trial application, protocol amendments, notification, and submission processes, as well as regulatory compliance. She has experience and knowledge of managing submissions and tracking approvals, reviewing and evaluating adverse event reports, creating and maintaining safety databases, reporting adverse events, managing safety issues, ensuring compliance, developing safety procedures and protocols, and ensuring the safety and efficacy of drugs and medical products. I strongly believe that Deeksha will be an excellent addition to a strong team in the pharmaceutical field.