Meet Lenia, Head of Regulatory Affairs at Adragos, Athens! In her role, Lenia oversees regulatory strategies and registration pathways for generic and generic plus developments, leading to over 200 successful regulatory applications across multiple countries. With a specialized focus on Value Added Medicines, her contributions lay the groundwork for products that not only meet regulatory standards but also deliver enhanced value to patients and healthcare providers alike. This track record underscores the commitment to ensuring the timely and compliant entry of pharmaceutical products into the market.

Lenia also provides valuable guidance in the initial stages of product development, emphasizing quality characteristics and regulatory compliance. She actively engages with major European Regulatory Agencies, contributing to scientific advisory meetings and referral procedures. Her expertise and contributions have made her a respected figure in the industry, facilitating access to essential medicines for patients across Europe.

Lenia Papadimou is a highly experienced professional with a solid educational background and over 25 years of dedicated service in the Pharmaceutical Regulatory field. With a BSc in Chemistry and an MSc in Pharmacy, Lenia has continually demonstrated her expertise and leadership abilities throughout her career. For the past 13 years, she has held the position of heading the Regulatory Affairs department at Adragos Athens, previously known as Lamda Laboratories.