WEBINAR SERIES

How to manage mandatory communication of Toxicological risks?

This webinar provides invaluable information on how to address and manage toxicological risks in the pharmaceutical industry, emphasizing the importance of timely and transparent communication.

 

Description

When a toxicological risk is identified in a pharmaceutical product, whether during the manufacturing process or at the finished stage, it is crucial to promptly take appropriate action and formulate priority strategies to safeguard the safety and quality of the product. In this webinar, we will delve into essential strategies for accurately assessing and interpreting such risks, effectively reporting and communicating findings, investigating root causes, and implementing corrective measures to mitigate and prevent potential harm to both patients and the environment.

What you'll learn

Speaker

Dominiek Rossillion

Dominiek Rossillion

As the Division Head of Quality Assurance at the QbD Group, based in Belgium, Dominiek brings extensive expertise to the table. He graduated as an Industrial Engineer in Chemistry (minor Biochemistry) and has over 17 years of experience in the life sciences sector. Throughout his career, he has held various roles in manufacturing (Quality, packaging, tech transfer, qualifications, …) and set up multiple successfully accredited QMS systems (ISO9001, 13485. GDP …). After gaining experience in sales, he now leads a team of 90 experts worldwide as the head of the QA Division.

Know more

Speaker

Patricia Lugo Mariani

Patricia Giulietta Lugo Mariani

Meet Patricia, our Toxicology Coordinator at the QbD Group. She’s got quite the academic background. She graduated  in Chemical engineering with a Master’s degree in Advanced Therapies and Biotechnological Innovation. She’s currently pursuing a PhD in Toxicology and Pharmacology at Complutense University of Madrid.

Patricia has a wealth of experience in microbiological research, including cell cultures, recombinant drugs, and physico-chemical lab work. She’s skilled at characterizing molecules, identifying impurities, and conducting CMC analysis. Additionally, she’s an expert at writing reports for regulatory agencies and has received GMP training. She’s also experienced in EMA and FDA audits.

Know more

Share with a colleague

Email
LinkedIn
WhatsApp

Watch the video

Come visit our booth at CPHI Barcelona 2023

Come to see the QbD Group at stand #3G73 at CPHI Conference in Barcelona. And after the conference…Eat & Connect with lifescience professionals at our QbD’s CPHI Networking Drink.