Drug approval is the goal of the long process of drug development. Once preclinical and clinical trial data have been collected, a New Drug Application must be submitted to the regulatory authority ...

Partnership formation is the new trend in common technical document development. Pharmaceutical and biotechnology companies are finding new innovative approaches to partnering with clinical research ...

Become more confident in your daily practices by gaining a deeper understanding of the US and European regulatory requirements for Module 3 (CTD) of your application.

LAHORE: Counter-Terrorism Department (CTD) of the Punjab police on Monday claimed to have busted a major terror module in the Rajanpur district of the province and ...

The author describes several issues in creating drug master files and active substance files for active pharmaceutical ingredients and intermediates. This article covers the submission requirements ...