OR WAIT null SECS
March 02, 2020
Emergency action to protect patients and the drug supply may have long-term implications.
No matter why change may be needed, it is important to comply with all the relevant regulatory requirements, says Siegfried Schmitt, PhD, vice-president, technical, Parexel Consulting.
Despite increasing R&D budgets by bio/pharma companies, returns on this investment are reducing and the cost of bringing an asset to market is increasing.
February 02, 2020
Bio/pharma researchers mobilize to diagnose and treat patients in pandemic threat.
January 02, 2020
The promise of new therapies is tempered by the need for affordability, safety, and ethics.
As a new decade has begun, this editorial reviews some of the biggest, brightest, and boldest happenings from the industry over the past 10 years.
December 02, 2019
Nearly four decades after the first diagnosis, the fight to treat HIV/AIDs continues.
As the UK heads to the polls for an unusual December general election, industry issues manifestos on medicines while Europe rejoices some movement … finally.
November 12, 2019
In batch production, efficient exception management means reducing the time required to identify, review, and resolve process exceptions. Incorporating review by exception functionality within manufacturing execution system (MES) software can streamline biopharmaceutical product release.
November 02, 2019
FDA report says drug shortages are underappreciated and patients pay a price.