January 27, 2017
Published by Doctor Dan at January 27, 2017
For the undiscerning, biosimilars in pharmaceuticals may sound like pharmaceutical generics, but they are different. The major difference is that biosimilars are manufactured, […]
January 17, 2017
Published by Doctor Erick at January 17, 2017
Pharmacovigilance or drug safety is the discipline in clinical research that deals with assessing, monitoring, and reporting whether pharmaceutical products being tested for […]
January 16, 2017
Published by Doctor Erick at January 16, 2017
What is Pharmacogenomics It is that field of scientific study where pharmacology and genomics combine to discover the responses of an individual to […]
January 9, 2017
Published by Doctor Erick at January 9, 2017
Microbiological methods are used for detection of microbial organisms in processes and procedures that require a sterile environment free of microorganisms. The procedures […]
January 5, 2017
Published by Doctor Erick at January 5, 2017
Drugs that are not approved by authorities like FDA and other federal authorities are considered unapproved drugs. FDA checks for the effectiveness and […]
January 4, 2017
Published by Doctor Erick at January 4, 2017
The organ-on-chip technology is a customizable chip that has inbuilt facilities to enable the mimicking of the responses of organs or organ systems […]
January 2, 2017
Published by Doctor Erick at January 2, 2017
ISSR is a comprehensive and detailed analysis about the safety of drugs in development. Although it is termed a summary, it includes a […]
December 29, 2016
Published by Doctor Dan at December 29, 2016
Drug development refers to the stages of drug research and discovery that bring the newly discovered drug to the market with regulatory approval.
December 23, 2016
Published by Doctor Erick at December 23, 2016
Patient safety in clinical trials has become prominent in the priorities of clinical research organizations (CRO) and other sponsors. In lieu of this […]
December 15, 2016
Published by Doctor Dan at December 15, 2016
Preclinical development processes for biopharmaceutical products refer to drug discovery, drug research and experimental testing on life forms other than humans that occur […]
December 8, 2016
Published by Doctor Erick at December 8, 2016
Drug safety or pharmacovigilance, as it is formally termed, is the field of science that is responsible for assessing, identifying and recording the […]
December 1, 2016
Published by Doctor Dan at December 1, 2016
According to the food and drug agency (FDA), sterile drug products are manufactured by two methods. They are terminal sterilization and aseptic processing. […]
November 25, 2016
Published by Doctor Erick at November 25, 2016
When a healthy volunteer/patient suffers a negative health reaction to a drug being tested in clinical trials, an adverse event is reported and […]
November 23, 2016
Published by Doctor Dan at November 23, 2016
When a patient/volunteer being administered a drug under clinical trials or outside trials in the case of a treatment regimen, undergoes an adverse […]
November 14, 2016
Published by Doctor Erick at November 14, 2016
The FDA aims to protect the health of U.S citizens’ by assuring them safe and secure drugs as well as biologics. However, the […]