Creation of medical content for different audiences, including healthcare professionals and the general public. Able to translate complex information into clear and accessible language, ensuring accuracy and adherence to best medical communication practices.
Preparation of presentations, information leaflets and training materials. including carrying out literature research and creating content.
Literature research and writing blog articles from peer-reviewed randomized clinical trials to inform and guide the use of anti-aging supplements.
Editing, reviewing and annotating references in promotional and non-promotional materials used by pharmaceutical companies ensuring medical accuracy and regulatory compliance.
Preparation of safety reports for clinical trials, including the analysis and compilation of data on adverse events and drug reactions. Ensuring compliance with international regulations, focusing on the accuracy and clarity of information to support decision-making and submission to regulatory agencies.
Preparation of Investigator Brochures for clinical trials, compiling clinical and non-clinical information on investigational medicines. Responsible for writing and organizing pre-clinical data, previous clinical studies, pharmacology, toxicology, efficacy and safety, ensuring compliance with regulatory guidelines (ICH-GCP).
Literature review, data extraction and analysis, and creation of technical reports to support the development of a new product.
Comprehensive literature searches, data extraction, data analysis, and creation of executive summaries to support decision making.
Consultancy (in-person) to develop and validate the Western Blotting methodology in an experimental neuroscience laboratory, including adapting the experimental protocol, preparing reagents and conducting initial tests.
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