Advance your regulatory strategy with confidence
Biotech Outsourcing Strategies Basel brings together biotech, pharma, contract research organizations, and contract development and manufacturing organizations to build partnerships and accelerate development-stage programs. With a strong focus on outsourcing across research and development and chemistry, manufacturing, and controls, the event creates opportunities for strategic collaboration and high-value conversations.
Meet with Cencora’s regulatory affairs and regulatory chemistry, manufacturing, and controls experts to discuss how to:
Meet with Cencora’s regulatory affairs and regulatory chemistry, manufacturing, and controls experts to discuss how to:
- Navigate evolving global regulatory requirements.
- Strengthen submission readiness across development and chemistry, manufacturing, and controls.
- Align external partners with regulatory expectations.
- Reduce risk and support more efficient development timelines.
Connect with our team at Booth 14 onsite in Basel
Anna-Lena Amend
Senior Manager, Regulatory Affairs, Cencora
Jaqueline Schaller
Director, Regulatory Affairs CMC, Cencora
Soubhik Banerjee
Director, Global Consulting Services - Global Strategic Accounts, Cencora
Angela Bonich
Manager, Global Consulting Services - Global Strategic Accounts, Cencora
Regulatory expertise for outsourcing success
Outsourcing can create speed and flexibility, but it also introduces complexity across functions, systems, and partners. Cencora helps biotech and pharma companies build stronger regulatory alignment across development and chemistry, manufacturing, and controls so they can move programs forward with greater clarity and control.
Our integrated regulatory affairs and regulatory chemistry, manufacturing, and controls capabilities help organizations:
Our integrated regulatory affairs and regulatory chemistry, manufacturing, and controls capabilities help organizations:
- Define global regulatory and chemistry, manufacturing, and controls strategies.
- Strengthen investigational new drug, clinical trial application, and marketing authorization application planning and documentation.
- Coordinate contract research organization and contract development and manufacturing organization activities with regulatory expectations.
- Identify potential gaps early and mitigate risk before they affect timelines.
Additional resources
White paper
Essential guide to post-approval regulatory lifecycle maintenance
Growing regulatory complexity and cost pressures are making it harder for biopharmaceutical companies to sustain post-launch revenue. Many are strategically outsourcing regulatory lifecycle management for established products to reduce compliance risk and costs while freeing internal teams to focus on strategic priorities.
Case study
Outsourcing excellence drives growth for specialty pharmaceutical developer
A growing specialty pharmaceutical company with 10 brands across six therapeutic areas needed a partner to optimize its cost model with global and in-country expertise. Cencora now provides full regulatory and pharmacovigilance maintenance services, helping reduce costs, increase flexibility, and free the company to focus on core priorities.
Connect with us at BOS Basel
For regulatory leaders, strong alignment helps reduce complexity, improve submission readiness, and support confident decisions across development. Schedule time with our team at BOS Basel to explore how Cencora can help streamline coordination and reduce regulatory risk.