Upcoming Events
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March 2021
ToxExpo 2021
The SOT Annual Meeting is the largest meeting of its kind. This annual event features a broad range of scientific sessions and a thematic program that provides participants with a unique opportunity to deepen their knowledge in topical areas and interact with leaders in their respective disciplines. The scientific program includes Plenary Lectures and other featured sessions, Symposia, Workshops, Roundtable discussions, Informational Sessions, and a Regional Interest Session, as well as Platform and Poster Sessions. The Society anticipates that more…
Find out more »Inhalation Drug Delivery Systems
This two-day conference will examine regulatory compliance issues facing inhalation therapies and future directions in respiratory drug delivery research. Industry experts will provide insight and case studies from lessons learned in design, compliance and other key areas. Networking and panel discussion opportunities are available to learn from leaders and pioneers in the industry.
Find out more »April 2021
Combination Products 2021
Combination Products Virtual Summit 2021 brings together thought-leaders and decision makers from across the industry to explore current and future trends in Combination Product Delivery Systems. The event includes presentations, panel discussions and networking opportunities with experts from FDA and top pharmaceutical and device companies.
Find out more »May 2021
Extractables & Leachables Summit 2021
This two-day conference will examine the safety, quality, and regulatory issues involved in a wide array of contexts central to the pharmaceutical and biotech industries, including drug packaging and delivery components, single-use systems, medical devices, and parenteral drug products. In addition, we will focus closely on the keys to satisfying recent revisions to several applicable USP chapters and the recently revised standards contained in ISO 10993.
Find out more »November 2021
Extractables & Leachables – West Coast 2021
This two-day conference will examine the safety, quality, and regulatory issues involved in a wide array of contexts central to the pharmaceutical and biotech industries, including drug packaging and delivery components, single-use systems, medical devices, and parenteral drug products. In addition, we will focus closely on the keys to satisfying recent revisions to several applicable USP chapters and the recently revised standards contained in ISO 10993.
Find out more »
