My Motivator and Objectives

The center of all my work is the desire to empower my clients to recognize and access products or technologies that are most appropriate, innovative, and safe for their business. It is pivotal for me that their selection of new or revised products is based in awareness of their responsibility and freedom to make their own choices. 

For me it is understood that every individual’s choice should be respected by everyone else.  

Experience

My professional experience of over 20 years includes a broad range of regulatory activities in the fields of medical devices, combination products, pharmaceuticals, cosmetics, food supplements and their ingredients. In global roles for several pharmaceutical, orthopedic medical device, health care, and nutritional products companies, I was responsible for regulatory compliance of their leading brands across various markets including B2B, retail, pharmacy, and hospital.

My acquired skill set that works to my clients’ advantage include the following:

• translate regulatory insights into strategic concepts for success;

• develop and deliver regulatory submissions for success of new or innovative products in global markets;  

• lead regulatory projects, streamline organizational structure, and deliver effective results efficiently across a full range of regulatory requirements to meet consumer expectations;

• shaping and influencing EU health-related policies and legislations as a company representative in Industry associations such as the Association of the European Self-Care Industry (AESGP);

• understanding, through the lens of 10 years’ experience, the public pharmacy’s need to engage both the health care professional and patient/consumer;

• ongoing professional training to broaden my know-how, compelled by my interest in innovation and new technologies.