Now available on-demand!
Biosimilar drugs are an increasingly common component of drug therapy. However, these complex molecules have a unique classification system and special rules for dispensing and substitution, that differ considerably from traditional drugs.
Join us for an exclusive webinar as we demystify biosimilars, highlighting the challenges and opportunities that they create for pharmacies. Learn about interchangeability, regulations, and product solutions that can help pharmacies navigate the complex world of biologic drugs.
Speaker:
Mark Fulton, PharmD, MBA, BCNSP, NSC-II
Director, Product Regulatory Compliance at FrameworkLTC
Mark Fulton is a multi-credentialed pharmacist and business leader with 20 years of experience across a diverse industry background in both community and specialty pharmacy practices.
He is a board-certified clinical specialist in nutrition support, as well as a certified expert in the NCPDP SCRIPT standard.
In his role as Director, Product Regulatory Compliance, Mark’s influence spans across the product suite, where he leads the clinical and regulatory dimensions of the SoftWriters suite of products.
Heather Butler
Senior Quality Assurance Analyst at FrameworkLTC
Heather Butler has over 20 years of experience as a pharmacist. In her current role, she is responsible for performing accurate software product and system testing, working with and communicating with other departments to ensure the effectiveness and quality of product, and much more.
Heather understands all of the product features related to biosimilars and was highly involved with the product team in refining, implementing and testing the biosimilar functionality.