QD Drug Development Platform
Our QD 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.
The optimized product development plan and target product profiles are conveniently available in your project management tool of choice and Powerpoint
Product Development Plan
Target Product Profile Benchmark
Trial Overview
Streamline your clinical trials with our advanced insights and tracking 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, and 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 and potential issues, enabling proactive decision-making to keep your trials on track and within 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 health authority meetings.
Leverage advanced search functionalities and intelligent filters to quickly find the information you need, reducing research time and maximizing learnings. Our platform helps you identify potential regulatory hurdles early, enabling proactive planning and streamlined approval processes for your innovative therapies.
Pharm·ology ApS
contact@pharmology.dk
CVR: 45557898
contact@pharmology.dk
CVR: 45557898
