With over 25 years of average experience in the field of Biotech/pharmaceutical development/Government regulatory expertise.
By combining robust expertise, proprietary patented algorithms and existing regulatory knowledge of pharmacogenomics and pharmacovigilance and medical affairs we are able to design offerings to both the biotech/pharma sector and directly to patients to allow them to manage their choice of medications and increased their awareness when managing their disease with their health care partnerships.
Due to the increased of regulatory scrutiny and digital health initiatives worldwide Medgenie is at the forefront of innovation in the field.