Michael De Cicco Email & Phone Number

Mirabel, Quebec, Canada

• Efficiently and effectively manage projects within scope of proposed time and budget, providing continuous project management training to junior team members.• Collaborate with key corporate stakeholders and external partners on scientific issue resolution and development of innovative ideas for products.• Direct and manage internal scientific affairs activities and communication with relevant stakeholders, including providing recommendations in support of business goals;•Spearheaded projects to obtain crucial licences under the Cannabis Regulations and Natural Health Product Regulations; • Primary contact for several government agencies.

• Prepare regulatory submissions to various health authorities (Health Canada, FDA, EFSA, TGA).• Ensure post-market compliance with global markets (mainly Canada, US, European Union, Australia) and communicate with their respective health authorities.• Ensure maintenance of regulatory certifications and permits. • Perform risk analyses for safety and regulatory issues. • Manage surveillance of ongoing scientific research and international regulatory developments. • Conduct literature reviews for Class III PLAs and clinical trials. • Review and critique pre-clinical and clinical study design protocols, data analysis, and preparation of reports.

Master Of Science (M.Sc.), Cell/Cellular And Molecular Biology

Bachelor'S Degree, Specialization Biochemistry