We organised the Webinar “Current and Future Trends in GxP”, with the participation of our Scientific Director, Sergio Scaccabarozzi, and our GLP Auditor Michelle Anderson.
The Webinar was full of insights. We are pleased to share the recording of the Webinar:
About the Webinar
The webinar will provide a comprehensive overview of the current and future trends in Good Practices (GxP) within the pharmaceutical, biotechnology, and medical device industries.
We will begin by establishing a foundational understanding of GxP principles and their importance in ensuring quality and compliance in the life sciences sector.
The focus will then shift to an exploration of the current trends shaping GxP, including the impact of technology, regulatory changes, and industry-specific developments.
The webinar will conclude with a forward-looking discussion on the future trends in GxP, highlighting the potential challenges and opportunities that these trends present.
Who is the Webinar for?
The webinar is ideal for professionals involved in quality assurance, regulatory compliance, and operations within the Life Sciences sector.
Overall, the webinar is relevant to a diverse audience within pharmaceutical, biotechnology, medical device, clinical research, and related industries, encompassing both technical and regulatory aspects of GxP compliance.
What will the attendees learn during the Webinar?
Attendees will gain valuable insights into how they can effectively prepare for and navigate the ever-evolving landscape of GxP compliance. By staying abreast of the latest regulatory developments, emerging technologies, and industry trends, participants will be better equipped to anticipate and address potential compliance challenges and spark internal discussion within their organizations.
Q&A Session
A Q&A session is scheduled at the end of the presentations.
Moderator
Sergio Scaccabarozzi
With a medical degree and a specialization in general surgery from the University of Milan, Sergio Scaccabarozzi has 35 years of experience in Clinical Research for global pharmaceutical and biotechnology companies.
In his professional life, Sergio spent 12 years as Head of Clinical Operations for the Italian affiliate of a big pharma and biotechnology company, managing a team of 90+ people and more than 220 studies from Phase I to Phase IV, RWE and providing support to institutions for Investigator initiated studies.
Sergio Scaccabarozzi enriched his professional experience by spending one year and a half as Operation Research Manager in one of the most important public research hospitals in Italy.
Sergio Scaccabarozzi is a member of scientific societies and working groups on Clinical Research, a recognized speaker at national and international events, with active editorial activities on Clinical Research and Life Science in general.
Speaker
Michelle Anderson
After many years of experience working in a variety of laboratories both in academia and for CRO’s, Michelle Anderson was the Quality Assurance Manager for a CRO, in which she managed all aspects of the Quality Management System, ensuring regulatory compliance of ISO 9001:2015, conducting internal and external audits as well as managing customer complaints and problem solving.
Before joining Arithmos’ UK Quality Assurance Team as GLP Auditor, Michelle was a GLP Auditor for a global life sciences and healthcare company.
About Arithmos
We are experts in the Life Sciences industry & Technology.
We help companies to gain the best business value through technology-enabled solutions and achieve excellence in business operations.
We are a long-standing partner for technology and expert service provider across Clinical, Regulatory, Quality, Pharmacovigilance and Medical Affairs domains.
