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Firma facilitates better patient experiences and trial diversity with global home trial services – and underpins this expert work with statistically sound data and analyses you can count on. All to help you accelerate the development of safe and effective treatments worldwide.
Change is inevitable throughout clinical development. Engaging in a partnership with Firma enhances your ability to respond to change and get to market as efficiently as possible.
Firma leaders have extensive experience across all aspects of the global drug development sphere. Our unique structure allows us to provide accountability and expertise to your project from a dedicated executive team member and a thorough medical review from an on-staff MD committed to scientific and operational alignment for your full project lifecycle.
Firma promotes savings with risk-based and data-driven monitoring, as well as a case-by-case implementation of data-centric and responsibility-centric methodologies. We provide a thoughtful and purposeful approach to every project by integrating data-centric processes with clinical expertise.
Firma acts as an extension of your team, relaying regular status updates as well as providing evidence-based recommendations to keep projects on track. We proactively initiate transparent, collaborative communication throughout the trial lifecycle. Intensive study-specific training, cross-functional communication, and superior study team education ensure we always keep your end goal in mind.
Industry experts that know your specific trial needs. Rapid EDC build times that beat industry standards. Cross-trained team members to knock down siloes. Custom-designed services. Firma’s flexibility allows us to consistently optimize time, cost, and quality for your study – and we’ve never missed a beat.
Make participation in clinical trial research easier and more valuable for patients – and produce higher-quality data – by partnering with Firma.
