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Advancements in personalized medicine and other innovations are transforming the way dosage forms are viewed.
This study aimed to develop a taste-masked drug resin complex using the ion exchange resin Kyron T-114.
Novel genetic engineering technologies are transforming the design and manufacture of bispecific antibodies, which are emerging as a promising new class of biologics.
June 12, 2017
The landmark decision determined that biosimilar makers can notify manufacturers before receiving FDA approval.
June 06, 2017
Takeda will build a new production facility at its existing Grange Castle site in Ireland.
June 02, 2017
As cost pressures mount as a result of multiple biologics being developed for the same indication, manufacturers can harness process efficiencies to maintain the value of legacy products.
Follow guidelines for E&L studies of an orally inhaled and nasal drug product formulation in its delivery device.
May 30, 2017
BioVectra will open its new microbial fermentation and complex chemistry site, including the capability to handle high-potency APIs, by the end of 2017.
The pharmaceutical industry is making efforts by internally assessing, developing, and implementing semi-continuous manufacturing processes to improve manufacturing efficiencies.
The company will expand its production facilities in Carlow and Cork to meet increased global demand for its medicines and vaccines produced in Ireland.
May 23, 2017
CBER is moving forward with the development and approval of regenerative medicine advanced therapies.
May 22, 2017
Ablynx will receive EUR15 million in milestone payment following Merck’s decision to advance ALX-1141 into clinical development. The nanobody was developed by Ablynx under a 2011 collaboration between both parties.
May 16, 2017
Saneca has been granted approval to manufacture and supply multiple dosage forms to Russia.