May 8, 2019
TRiNDS is dedicated to clinical trials and research for
people with neuromuscular and other rare diseases. Rare disease research is
evolving quickly – the science is complex, the populations are small, and
everyone wants to finish trials quickly. It takes a team of experts to reach
rare disease research goals.
TRiNDS is guided by an expert board of advocacy group
leaders, researchers, and clinicians who help us do our best work for our
clients. The experts on our board bring perspectives from industry, academia,
major clinical centers, and non – profit groups. We rely on them to help steer
our work in the right direction. This
week, our teams are travelling to the main TRiNDS offices for our annual
company – wide meeting. We’ll be taking time to reconnect, to reflect on our
accomplishments, and to plan for the year ahead.
Are you starting a rare disease research project in 2019? Email us to learn how our unique business model can support your projects’ success.