Allison Jones
Seminars
Wednesday 17th March 2027
Strengthening Pharma–CDMO Collaboration to Navigate Environmental Regulations & Achieve Shared Sustainability Goals
3:45 pm
- Address environmental compliance challenges when pharma sponsors dictate materials and manufacturing processes, while CDMOs must manage the resulting site-level risks and regulatory obligations
- Strengthen sponsor–CDMO communication to anticipate regulatory changes, assess manufacturing capabilities and secure the capital investment needed to maintain compliance
- Align EHS, sustainability and operations teams across the supply chain to eliminate conflicting priorities, coordinate environmental improvements and meet shared compliance and ESG targets
Wednesday 17th March 2027
Roundtable Discussion: Navigating PFAS, RCRA & Emerging Environmental Regulations to Mitigate Compliance Risks & Future-Proof Biopharma Operations
4:15 pm
- Explore regulatory hot topics including PFAS restrictions, RCRA waste management requirements, and emerging environmental regulations affecting biopharma
- Learn strategies for proactive compliance monitoring and preparing your organization for regulatory changes before they become mandatory
- Gain insights into environmental aspects of laboratory operations and how to integrate environmental considerations into R&D and manufacturing processes
