EMA committee endorses Takeda dengue vaccine candidate
Takeda’s dengue vaccine candidate has been recommended for approval by an EMA commitee.
Takeda’s dengue vaccine candidate has been recommended for approval by an EMA commitee.
The US Food and Drug Administration (FDA) has extended the review period of the new drug application (NDA) for Biogen’s tofersen: with a decision now expected in April next year.
Charles River Laboratories International has launched a new AAV based platform that it claims has the capability to reduce time from process development to GMP by 55% and deliver a drug product in fewer than eight months.