Ideagen Huddle for life science
Ideagen Huddle provides every team, from research to sales, across life science and biopharma with a single source of truth that powers break-through innovation.
As Huddle is so easy to navigate, everyone was on board right away.
Request a demoExperience the benefits of Huddle with a free demo
Life sciences can improve lives faster
Life science and biopharma organisations work tirelessly for years to perfect the drugs and devices that will improve patient outcomes. When innovating is a crucial element of the process, something as simple as the collaboration process should slow down those efforts.
With Huddle, you can make faster but higher quality decisions right from the beginning of your R&D stage through to post clinical trials, marketing, and sales. When you collaborate on your most important documents and manage them effectively, you make success the standard.
Compliance first approach
With regulatory requirements fast becoming more stringent, there is a growing need for companies to mitigate risks by quickly finding sensitive information. With Huddle you can head off challenges by auditing as you go along and be confident you can find and solve mistakes when they crop up.
Leave confusing collaboration behind
When your work is stored in one place, you make it easy to collaborate with external clinical research organisations (CROs) and partners across the world. Every time you need to work on a document together, you can always find it in the same place and be confident that it is the latest version.
Protecting your I.P.
Your ideas and plans are the life blood of innovation. Safeguard your organisation with a single source of truth to protect your greatest assets. Show GxP by safeguarding your research, ideas, polices, processes, procedures, reports and more in a simple but effective single source of truth.
Dicerna Pharmaceuticals turns to the cloud to collaborate with partners worldwideRead case study
The single source of truth for life science
Kick off collaboration on projects no matter where you are. You can hit the ground running by being able to easily find verified documents, FDA forms, site feasibility surveys and approved files.
Quality document management
Make quality and GxP the standard when controlling the lifecycle of all your documents. From planning and first drafts to sharing final policies, reports SOPs and Wis.
Clinical data management (CDM)
Produce high quality, reliable, and statistically sound data from clinical trials which can be securely shared with stakeholders, sponsors and CROs.
Controlled collaboration between CROs and CMOs
Put secure controls in place between all stakeholders, CROs and CMOs when sharing sensitive data and strategy proposals across the supply chain. Make sure that only those who need to see the data have access.
The first to launch
Fast track your product launches, without compromising on quality, by collaborating on promotional materials and making final assets available to marketing, sales, and field teams.
Carry on through mergers
Integrate teams and be cut out the delay when M&A activity takes place. Stalled projects can cost billions so transition knowledge as quickly as possible with a single source of truth.