Translational Toxicology: Biomarker Development

Biomarker use in translational medicine is predicated upon preclinical qualification and validation – 2 distinct steps in the biomarker development process. ivermectina tiene penicilina   Prior to issue in 2009 (EMA) and 2010 (FDA, PMDA) of the renal-specific...

Drug Abuse Liability Testing

Any new drug that penetrates the central nervous system must receive some preclinical analysis of abuse liability potential (Draft Guidance).  Usually, it is determined through prior knowledge of chemistry and/or pharmacology of the candidate’s drug class that...

Turbulent Blood Flow may Increase Cardiovascular Risk

By utilizing the basic principles of hemodynamics and hydraulics, research suggests that fluid retention is detrimental for the cardiovascular system because it increases the likelihood of turbulent blood flow, regardless of whether or not blood pressure is raised....

FDA Strengthens the Science of Regulatory Safety

In order to keep our competitive edge, the Federal Drug Administration (FDA) is placing increased emphasis on strengthening both the field and application of regulatory science relative to pharmaceutical research, development, review, and post-market surveillance. ...

Dried Blood Spot Analysis: Preclinical Pros and Cons

Both advantages and challenges exist for use of dried blood spots during preclinical drug development. سلوتس اون لاين    Advantages include small sample volumes coupled with easy shipment and storage.  The amount of blood per spot varies (10 to 100 μL), but use of 15...

Personalized Medicine: Friend or Foe?

For pharmaceutical companies, is personalized medicine more of a threat than an opportunity? ivermectin horse dewormer dose for dogs   In addition to the development of new drugs, genetic information can also help target the use of current medications (e. how soon...