To ensure the implementation and regulations for the registration, certification, pricing and reimbursement and marketing of products;
To define the strategy and planning of registrations and applications for inclusion on the list of reimbursable medicines for both retail and hospital products;
To organize and supervise the regulatory activities, Marketing Authorisations and price applications for all Ferring products, in accordance with the requirements of Health authorities;
To ensure the strict compliance to Public Health Code in relation to the monitoring of Ferring product’s safety and particularly on the requirements of Pharmacovigilance;
To organize and monitor all pharmaceutical operations of the company (manufacturing, secondary packaging, storage operations, import, distribution, export, batch follow-up, withdrawal and recall of batches;
To control promotional communication of all Ferring France products and their environment;
To implement and maintain quality policy (ISO certification, sales force certification);
To perform regulatory business intelligence and participation in the development of legal files;
To ensure monitoring of safety of the products involved in local clinical trials, post marketing surveillance and materiolovigilance;
To ensure the quality of responses to medical questions from health professionals and patients.
Expertise in specific issues within pharmaceutical industry (medical and ethical constraints – DMOS-, medical advertising regulations);
Know-how in economic management of the company;
Knowledge of the ISO rules;
Ability to analyse and monitor data related to products.