Vigipharma Consultancies Ltd Reliability in drug safety, medical regulatory affairs and research

Our company provides tailored-made solutions to pharmaceutical companies and individuals in medical regulatory affairs, pharmacovigilance, medical device vigilance, pharmacoepidemiology, Clinical Trials, and medical research. In terms of regulatory compliance, we provide our clients with the local and global regulatory submissions requirements so they can achieve regulatory compliance. We also provide insight to pharmaceutical companies to establish and maintain their pharmacovigilance system and can act as the local single point of contact for regulatory authorities on a 24-hour basis for pharmaceutical companies who may need a local Qualified Person for Pharmacovigilance. We also provide guidance on carrying out internal mock audits of pharmacovigilance systems as well as inspections. With more Subsaharan African countries strengthening their national medical regulatory agencies, our company can digitalize and make submissions easier and faster hence ensuring the safety of medicines