Indian pharma exudes confidence to sustain US market presence under President Trump’s regime: Nandita Vijayasimha, Bengaluru Thursday, January 23, 2025, 08:00 Hrs [IST] Indian p ...
Moreover, most of the existing databases (i.e., OMIM, Human Gene Mutation Database (HGMD), CTD, and PharmGKB) which curate pharmacogenomics relationships employ manual curation of biomedical ...
Submitting a Carcinogenicity WoE document prior to the New Drug Submission (NDS ... it should be placed in Module 4.2.3.4 of the Common Technical Document (CTD) structure. It is also recommended that ...
The "Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application Training Course" conference has been added to ResearchAndMarkets.com's offering. The Common ...
From 31st January, 2025, all clinical trials in the European Union (EU), including ongoing trials that were approved under the previous legal framework, the Clinical Trials Directive (CTD), are ...
Over the past nine years, patients with spinal muscular atrophy have seen the number of FDA-approved treatment options for ...
U.S. District Judge John D. Bates granted a restraining order temporarily reversing the Trump administration’s moves to ...
Short chains of amino acids can form drug delivery nanoparticles and boost the properties of potential medicines ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback