Panel: Identifying TMF Best Practices for the Small to Mid-Size Biotech Company & Large Pharma on a Budget

Session details:

For small to mid-size biotech companies and even large companies with tight budgets, ensuring compliance with Trial Master File (TMF) regulations can be challenging due to limited resources, evolving processes, and increasing regulatory expectations. However, by implementing best practices, these companies can maintain an inspection-ready TMF, improve efficiency, and support the successful execution of clinical trials. In this session, we will share these best practices that will not only be important to small to mid-size organizations but also for large organizations looking at ways they can improve cost and operational efficiencies.