Combination products are complex by definition, and the product development cycles can be both time- and resource-intensive. The common theme of challenges has been ...

There’s an important person out there influencing your next oncology trial patient. We don’t often talk about this person within clinical research, much less plan fo...

Study oversight is a broad topic. We have reviewed how site performance and clinical data controls can be implemented across various monitoring techniques as well as...

Big data combined with advances in data science approaches have provided a valuable opportunity for the pharma industry to uncover previously unobtainable insight th...

Six simple but effective steps to set the TMF in the right direction The clinical trial master file (TMF) is a bit of a misnomer, in that it is not really one fil...

By reducing enterprise systems into three key services of data management, information security and data access, we can solve many of the current challenges faced in...

Tablet compression tools are often viewed as consumable items; therefore, maintenance can be seen as unnecessary and time-consuming. This can be a costly mistake and...

The development of a dissolution method with suitable specifications is a key part of any oral drug product control strategy. Dissolution testing is an in vitro tech...

Ophthalmic pathologies include eyesight-threatening conditions (diabetic retinopathy, glaucoma, cataract, age-related macular degeneration and retinal detachment) an...

Way back prior to 2016, Brussels Airport, Miami International Airport and Singapore Changi Airport came together with the joint ambition of fostering greater collabo...