Join the first webinar of our series on the WHY, HOW, WHO, WHAT and WHEN of Regulatory Writing on Thursday 16 January 2025. In this webinar, we will be covering the general aspects; giving you a brief introduction into regulatory affairs and the documentation required...
Join our second webinar of the series on the WHY, HOW, WHO, WHAT and WHEN of Regulatory Writing on Thursday 6 February 2025. Following our first webinar on general aspects on Thursday 16 January 2025, this webinar will delve deeper into the various documents required...
Join our third and final webinar of the series on the WHY, HOW, WHO, WHAT and WHEN of Regulatory Writing on Thursday 27 February 2025. This webinar will delve deeper into the various documents required for early development and highlight the importance of involving skilled...
Turn Drug Development Theory into Actionable Strategy The road from concept to first-in-human trials is filled with complex decisions. Understanding how CMC, clinical, and non-clinical aspects connect is critical—but theory alone won’t get your product to the next stage. This hands-on workshop is designed to...
Drug development is complex. Plans look great on paper, but execution is another story. Unexpected challenges, regulatory hurdles, and resource constraints can turn even the best strategies into roadblocks. That’s where Venn Workshops come in. This hands-on workshop series is designed to bridge the gap...
