QD Drug Development Platform

QD Drug Development Platform
The QD [Quantify Decisions] Drug Development Platform offers a comprehensive and integrated solution for accelerating drug development and regulatory approval, from first-in-human clinical trials to regulatory submission, leveraging our cutting-edge technology and expertise.
A robust product plan, outlining the critical development path, and a target product profile (TPP) are vital for timely strategic decision-making in drug development.
That is why we developed the QD platform integrating these essential tools with totality of available evidence from regulatory submissions, competitor results, and clinical trials to secure your optimal decision-making.
Christoffer Wenzel Tornøe, Founder of Pharm·ology
84,649
Industry Sponsored Clinical Trials
11+ million
Outcome & Adverse Event Measures
184,536
FDA Regulatory Submissions
Trial Overview
Streamline your clinical trials with our advanced insights capabilities. Our platform provides a centralized hub for all trial-related information such as trial site locations, treatment duration, recruitment speed, patients enrolled and their baseline characteristics, primary and secondary endpoints, drop-out rates and reasons ensuring seamless trial program strategies and planning from start to finish.
Our intuitive dashboards and reporting tools allow for identification of trends, enabling proactive decision-making to plan trials with competitive timelines.
Competitor Insights
Stay ahead of the curve with our robust competitive insights module and market analysis capabilities. Our platform provides in-depth insights into your competitors' product pipelines and efficacy and safety data, enabling you to make quantified strategic decisions.
Leverage comprehensive QD reports to understand what it takes to be best- or first-in-class, identify opportunities, and mitigate risks. Our tools help you pinpoint areas for differentiation and innovation, ensuring your drug development efforts are aligned with market needs and competitive advantages.
Regulatory Explorer
Navigate the complex landscape of drug development regulations with our intuitive Regulatory Explorer. 
This powerful tool provides access to all FDA approved drugs and biologics, ensuring your projects can leverage prior knowledge from supplements, reviews, labels, and Q&A from health authority meetings.
Target Product Profile
Elevate your product's trajectory with the Target Product Profile (TPP) module. Enhance your strategic decisions on product positioning, regulatory labels, and key differentiators by rigorously benchmarking your asset's data and aspirations against competitor regulatory claims (indications, dosing, populations) and their clinical data (efficacy, safety & tolerability).
Product Development Plan
Experience a product development plan designed for accelerating your time to market.  Navigate the complex regulatory landscape with confidence through our insights about health authority meetings and regulatory submissions.
Your optimized product development plan is not just a strategy — it's a dynamic, actionable roadmap, conveniently integrated into your project management tool of choice for seamless execution and tracking.
Pharm·ology ApS
contact@pharmology.dk
CVR: 45557898