Life Sciences & Clinical Research

Operationalising clinical research at speed and scale

Life Sciences & Clinical Research

Operationalising clinical research at speed and scale

Life Sciences & Clinical Research

Operationalising clinical research at speed and scale

Our platform is not hard coded, which makes it easier to create a study for your specific therapeutic area quickly and efficiently, and collect high-quality data specific to your TA protocol.

Combined with our deep domain expertise, our easy-to-build platform enables you to deploy a robust clinical trial at speed and scale for your particular therapeutic area. Achieve higher accuracy with continuous data collection and near real-time reporting.

Our platform is not hard coded, which makes it easier to create a study for your specific therapeutic area quickly and efficiently, and collect high-quality data specific to your TA protocol.

Combined with our deep domain expertise, our easy-to-build platform enables you to deploy a robust clinical trial at speed and scale for your particular therapeutic area. Achieve higher accuracy with continuous data collection and near real-time reporting.

Our platform is not hard coded, which makes it easier to create a study for your specific therapeutic area quickly and efficiently, and collect high-quality data specific to your TA protocol.

Combined with our deep domain expertise, our easy-to-build platform enables you to deploy a robust clinical trial at speed and scale for your particular therapeutic area. Achieve higher accuracy with continuous data collection and near real-time reporting.

Our platform is not hard coded, which makes it easier to create a study for your specific therapeutic area quickly and efficiently, and collect high-quality data specific to your TA protocol.

Combined with our deep domain expertise, our easy-to-build platform enables you to deploy a robust clinical trial at speed and scale for your particular therapeutic area. Achieve higher accuracy with continuous data collection and near real-time reporting.

Powering digital-first clinical research

Powering digital first clinical research

Powering digital-first clinical research

Ready. Set. Go.

Streamlined user journeys help accelerate time to “first patient in” and get your trial up and running with minimal fuss. Our fully integrated screening and consent workflows enable quicker, easier setup and enrollment. With less time spent on logistics, you’re free to focus on what’s truly at the heart of your clinical study: your participants.

Engaging. Efficient. Clinically proven.

Huma’s award-winning human-centered design has been developed with an understanding of the complex needs of patients and clinicians in mind, enabling us to impact each touchpoint across clinical trial phases. Now you can enroll participants faster and keep them engaged longer for better clinical trial outcomes.

Agile. Quick. Adaptable.

Mid-study changes are inevitable, but Huma makes things simple when they happen. Unlike hard-coded platforms, our highly adaptable platform is designed with flexibility in mind to enable near real-time modifications and additions to study protocols without having to go back to the drawing board.

Driving clinical research into the digital era.

As part of the Huma family, Alcedis’ unique approach combines full service clinical trial expertise with disruptive technologies creating significant advantages for patients, physicians and the life science sector. With over 25 years of experience, Alcedis pioneered data-driven studies from phase I through drug approval and beyond market access into real world evidence – aiming to create better outcomes for patients and to accelerate progress in human health.

Driving clinical research into the digital era.

As part of the Huma family, Alcedis’ unique approach combines full service clinical trial expertise with disruptive technologies creating significant advantages for patients, physicians and the life science sector. With over 25 years of experience, Alcedis pioneered data-driven studies from phase I through drug approval and beyond market access into real world evidence – aiming to create better outcomes for patients and to accelerate progress in human health.

Enhancing clinical research with AI.

Deeply rooted in clinical research, Alcedis Labs forms an integral component of the Alcedis IT department. Our primary mission involves tackling real-world challenges and designing AI software products that are instrumental in day-to-day clinical research activities. Through our extensive collaboration with various Alcedis departments, we consistently bring tangible value to our customers, prioritising their needs above all else.

Enhancing clinical research with AI.

Deeply rooted in clinical research, Alcedis Labs forms an integral component of the Alcedis IT department. Our primary mission involves tackling real-world challenges and designing AI software products that are instrumental in day-to-day clinical research activities. Through our extensive collaboration with various Alcedis departments, we consistently bring tangible value to our customers, prioritising their needs above all else.

Regulatory, safety and compliance

Regulatory compliance
International medical device standards
QMS & info security management
Technical documentation
Regulatory
compliance
International medical device standards
QMS & info security management
Technical documentation
Regulatory compliance
International medical device standards
QMS & info security management
Technical documentation
Regulatory compliance
International medical device standards
QMS & info security management
Technical documentation

Take the next step

Tell us what you’re working on and what you need from Huma to move forward.

Take the next step

Tell us what you’re working on and what you need from Huma to move forward.