Farida H.

Expert in RA affairs (pharma). 19 years' experience in various positions in pharma, including medical writing and translations. Enthusiast pharmacist. More than 250 successful RA projects in different countries, about 15 medical writings (Separate parts of Modules 2 & 3), and more than 20 medical translation projects. If you are looking for a proactive and experienced pharmaceutical regulatory affairs consultant, congratulations, you have found her! I am a pharmaceutical professional passionate about bringing innovative medicines closer to patients. With over 15 years in Market Access, drug registration, and pharma analytics, I’ve learned how to connect science, business, and data to achieve real impact. I enjoy coordinating projects, building bridges between teams, and turning complex challenges into clear solutions. My experience ranges from regulatory projects to market access strategies, and I thrive where pharmaceutical expertise meets data-driven decisions. One of my favorite tools is Power BI – it helps me transform numbers into stories and insights that support smarter choices for both companies and patients. I’m looking to contribute my knowledge and energy to projects that improve healthcare access, create value for stakeholders, and drive innovation in the pharma field.