Association for Accessible Medicines
601 New Jersey Ave NW, Suite 850
Washington, DC 20001
E: [email protected]
Alberto Rivalta is a Senior Director of North America Generics Regulatory Affairs at Teva Pharmaceutical USA. Prior to joining Teva, Alberto held various positions in analytical research & development and regulatory affairs at different companies. He joined Teva in 2001, and in his current role, he manages teams responsible for pre and post-approval activities for solid oral dosage form drug products, provides regulatory advice, and ensures quality applications are submitted to the Food and Drug Administration, with the scope of securing approvals. Alberto has 28+ years of combined regulatory experience.