The pharmaceutical, laboratory, and analytical industries are entering a defining phase where scientific rigor, technological intelligence, and regulatory expectations are converging like never before ...

While there is a need for accuracy in pharmaceutical research, there is even a greater need for speed. Recent advancements in research have focused on methods for maximizing speed while still allowing ...

For over 100 years, the major public health advances have been the result of major scientific discoveries. The ways in which new medicines are discovered and manufactured is undergoing as major a ...

Pharmaceutical science has always demanded precision. Small differences in a product can have major consequences, and identifying or preventing these differences often requires extensive and ...

Many people have made an outstanding contribution to the field of microbiology in the first two decades of this century and selecting ten is a difficult task. In selecting ten eminent researchers I ...

Microbioz India perform an interview with Dr.K.P. Ranjan,Department of Microbiology,Gajra Raja Medical College,Gwalior,M.P.,India,Dr.Ranjan is a Medical Microbiologist and have depth interest in ...

The key to making profits in the generic drug market is reaching the market as early as possible by getting proper regulatory approval. Generic medicines play an essential role in the pharmaceutical ...

For almost 20 years, custom medicine’s potential for success has been driven by the ability to potentially identify molecular signatures for a disease’s etiology instead of population-based markers.

In 1917, Kamal Ranadive was given birth to in Pune, India, where it was not normal to have a girl student in the sciences at Fergusson College. Luckily for Ranadive, her decision to go to college was ...

Based on the Threshold of Toxicological Concern (TTC) concept described in ICH M7 (1), most mutagenic impurities are limited to a dose of 1.5 µg/day which corresponds to a 10-5 excess lifetime risk of ...

Glycosylation, an important post-translational modification, is a key critical quality attribute (CQA) that influences product safety and efficacy and should be monitored when developing new ...

Pharmaceutical products are routinely manufactured under strict GMP guidelines. Despite these strict codes, as a fail-safe prior to batch release, all pharmaceutical products undergo stringent ...