SHELTON, CT / ACCESSWIRE / October 9, 2019 / NanoViricides, Inc. (NYSE American:NNVC) (the "Company") a leader in nanomedicines with novel platform technology to treat difficult and life-threatening ...

The MarketWatch News Department was not involved in the creation of this content. In this free webinar, learn about mRNA analytical platforms required for investigational new drug (IND) submissions.

LabZient™ combines predictive in-silico evaluation with well-established and vetted laboratory methods that de-risk the application of platform analytical procedures. In doing so, LabZient™ removes ...

In the pharmaceutical industries, validation of analytical methods is a critical process that confirms the reliability and appropriateness of a method for its intended application. Method validation ...

In today’s pharmaceutical environment, where compliance and speed-to-market are paramount, analytical method development and validation play a foundational role. From early research through to GMP ...

In this article, the author modestly expresses his views on the use and understanding of linearity, a key parameter to be determined in analytical method validation in quality control laboratories (QC ...

The "Analytical Methods in Fine Particle Technology" eBook provides a comprehensive overview of techniques and principles related to the analysis of fine particles, which are crucial across various ...

When evaluating a drug’s risk assessment for elemental impurities, one must consider all aspects of its lifecycle. A crucial step in achieving approval of a biosimilar is establishing analytical and ...

The attributes of the DS or DP that are to be tested to obtain the necessary information about product quality safety and efficacy are determined during the Drug Development stage. The information ...