Easier Regulatory Approvals. If you want to bring your innovative product to patients as fast as possible but you don’t know how to navigate France’s health care system productively (i.e.: ANSM: French National Agency for Medicines and Health Products Safety, and/or HAS: High Authority of Health). Pharmassent provides strategic support, tailored to the client’s needs, in addressing France regulatory affairs.
Our expertise in administrative compliance and project facilitation with ANSM practice can bring improved recognition to your brand and product. Pharmassent can review your product and help you prepare documents (CTD) for pharmaceutical approval.
You can rely on our expertise to get your products (drugs or/and medical devices) to the French and European market faster. Furthermore, we can help your company pre-launch global drug pricing and reimbursement registration procedures. With our experienced skill, we help you achieve greater sales success in the European market. We would be proud to help you with the entire regulatory process to meet your objectives faster.
