July 9th - 10th, 2019 (Philadelphia, PA)

6th Clinical Regulatory Medical Writing Forum

In order for a new drug or therapy to gain marketing authorization, writers must coordinate with various stakeholders to gather, organize and compile information on new products or processes; interpret data from clinical trials; and find efficient ways to present trial findings. These documents are then submitted to the FDA, EMA and other regulatory authorities for their approval, with very little time to respond to inquiries or provide additional information.

September 10th - 11th, 2019, Hilton (Amsterdam, Netherlands)

World Drug Safety Congress EU 2019

World Drug Safety Congress Europe was the first strategic pharmacovigilance event to unite a plethora of stakeholders in drug safety, from pharma and biotechs to regulators and patients.

The event continues to lead the way in moving the sector forward and has been running for over a decade. It is world renowned for its ability to connect key stakeholders and grow the industry. Join us and be part of the story!