The COVID-19 pandemic brought an enormous urgency to the life sciences sector. Companies vied for suitable treatments and in less than a year, COVID-19 vaccines were developed. This demonstrated clearly that the sector could move at speed when necessary. Though vaccines were supported by regulators, inefficiencies in vaccine and drug development were exposed.
However, the pandemic created a huge problem for people running clinical trials, especially existing trials. Routine health care visits were discouraged or even banned. Everything moved to online consultations. How can you carry out clinical trial assessments if you can’t visit patients, and they can’t visit you? How did the industry speed up vaccine development?
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