Navigating Animal Welfare Legislation in North America: Insights for Biotech & Pharma

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Sponsored by:

Certis Oncology Solutions, Inc.
Date:
January 22, 2024
Time (PT):
6:00 PM

Our discussions touch upon the defining regulatory mandates, industry best practices, and the overarching ethical directions that guide the treatment of animals within these industries. Coupled with expert opinions and thought leadership on North American compliance standards, we aim to shine a light on our crucial role in ensuring ethical standards aren't just met - they are exceeded.

Whether you're a professional aiming to broaden your knowledge, an organization looking to solidify its regulatory grasp, or simply an animal welfare advocate keen on learning more about our combined responsibility, this series certainly has something for everyone.

To access additional resources and handouts, please contact meaghan@scientist.com.

Head over to Part Two (Asia-Pacific) or Part Three (Europe) for more!

Presenters

Meaghan Loy

Scientist.com (In Vivo and GLP Services)
Senior Director

Meaghan Loy is currently the Senior Director of In Vivo and GLP Services at Scientist.com, a research marketplace that enables researchers to access pre-qualified assessed animal model suppliers as well as hundreds of suppliers that provide in vitro models that can potentially replace or reduce the use of in vivo models. She joined Scientist.com in 2018 and is an expert in the use of COMPLi®, Scientist.com’s award winning platform that introduces a common, comprehensive process and supply agreement supporting access to pre-qualified assessed suppliers of in vivo and in vitro research models and provides animal welfare compliance coverage.

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Megan LaFollette

The 3Rs Collaborative
Executive Director

Dr. Megan LaFollette is Executive Director at The 3Rs Collaborative where she advances better science, for both people and animals. Her expertise includes a wide range of topics including animal welfare, human-animal interactions, compassion fatigue resiliency, and even microphysiological systems. She is committed to advancing widespread implementation of practical, impactful, and evidence-based 3Rs techniques: refinement, reduction, and replacement.

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Diana Hornberger

Certis Oncology Solutions, Inc. (Regulatory and Quality)
Director

Diana Hornberger is the Director of Regulatory and Quality at <a href="https://www.certisoncology.com/#drug-development" target="_blank" rel="noopener">Certis Oncology Solutions, Inc.</a>, a specialty CRO with expertise in human pre-clinical cancer modelling. With 17 years of experience, she has expertise in regulatory compliance, quality assurance and control, vivarium management, animal welfare, operations, and In Vivo model development.

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Sponsor

Certis Oncology Solutions, Inc.

Certis explores options for precision therapies beyond the current standard of care, and partners with pharmaceutical companies to develop the next generation of targeted oncology therapeutics.

Content Partners

Scientist.com

Scientist.com is the world’s largest and first platform built for the intricacies of scientific outsourcing.

We help pharmaceutical and biotechnology organizations discover, engage, manage, and scale relationships with the providers that support every stage of the pipeline—from discovery and preclinical research to clinical development, manufacturing, medical affairs, and commercialization. Through a centralized platform, organizations can access a global network of 6,000+ providers, streamline sourcing and procurement workflows, maintain compliance, manage supplier relationships, and leverage data-driven insights to make faster, more informed decisions.

Today, Scientist.com supports more than 130 life science organizations, including 24 of the world's top 30 pharmaceutical companies, helping teams reduce operational complexity, accelerate timelines, and bring innovations to patients faster. Our mission is to make it possible to cure all human disease by 2050.

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