Discovery & Preclinical
Set a clear product strategy, define a credible clinical and regulatory path, select the right asset and get ready for first-in-human trials with confidence
tranScrip's rich heritage in infectious diseases equips us with the necessary expertise to support clients in developing groundbreaking treatments for these critical health challenges.
Our team of ID experts, who have held senior leadership positions in both pharmaceutical and biotech sectors, are adept at integrating seamlessly as an extension of our client’s teams, providing support activities typically conducted by pharma in-house.
tranScrip’s expertise spans antibacterials, antifungals and antivirals. We support clients across all phases of preclinical and clinical development, including microbiology, PK/PD, design and oversight of clinical programmes, regulatory strategies and agency interactions, MAA/NDA submissions, peri-launch medical affairs and commercial activities, as well as in-licensing, fund-raising and due diligence activities.
We provide strategic expertise, therapeutic experience and operational excellence across the entire product lifecycle.
Set a clear product strategy, define a credible clinical and regulatory path, select the right asset and get ready for first-in-human trials with confidence
Implement first-in-human trials, interpreting emerging data and adapting plans as needed. Ensure robust decisions, including clear proof-of-concept
Design medically-endorsed pivotal programs that stand up to global regulatory and commercial scrutiny. Navigate issues in implementation
Interpret data, assess benefit/risk and secure regulatory approvals, successfully bring your medicine to market. Ensure strong lifecycle management
Chief Medical Officer
Destiny Pharma
Get in touch to see how our senior cross-functional experts can help you reduce risk, protect value, and move forward with confidence.