Daniela Rubini

Responsible for development, launch, roll-out and maintenance activities of OTCs, Cosmetics, MDs. 1.Define the strategy to develop, register and launch OTCs, MDs or Cosmetics in cooperation with clinical, non-clinical, marketing and legal divisions. 2.Drive the development of proper data to support new registrations 3. Evaluate the feasibility of projects worldwide based on countries requirements and data available 4.Coordinate worldwide regulatory activities for concerned product and projects

Regulatory Affairs Manager – Healthcare and Personal care brands; responsible for launch, roll-out and maintenance activities of OTC, SOP, Cosmetics, MD, general products. 1. Responsible for regulatory activities for concerned products and projects: 2. Organize the area of responsibility managing, training and developing person responsible for

Regulatory Affairs Officer – Medicinal products (OTC and RX), cosmetics and food supplements brands.

Drugs (marketed or investigational) adverse events monitoring – Oncology drugs

 Pharmaceutical Development and Scaling-up Laboratory (solid and semisolid formulations development; scaling up; handling of UV, RX, DSC, HPLC, dissolution test; annual review)  Contract manufacturing (transferring of production to external companies; technical agreements)