Study document processing, protocol drafting support and pharmacovigilance summaries, evaluated on documents you choose, with where the work runs agreed first.
Prefer email? hello@azitalabs.com, subject “Workload evaluation: Pharma & clinical research”
Your clinical research produces study documents, protocols and pharmacovigilance reports that need reading, extraction and summarising. Your SOPs and sponsor agreements keep trial data under your control, and sending it to outside tools fails your vendor qualification. So teams either avoid the tools or data ends up in tools nobody qualified, and the safety reviews queue.
An example workflow
Study reports are compiled from many site documents for each submission. An evaluation could extract data from documents the team releases and let its medical writers compare the output with their own, and the total cost.
An example workflow
Adverse event reports arrive in many formats and must be summarised consistently. An evaluation could summarise a sample of closed cases and let the safety reviewers judge accuracy before anything changes.
An example workflow
Screening results and literature need summarising for each programme. An evaluation could run one representative programme's documents where GxP rules and the lab's policy allow, and set the scientists' review next to the total cost.
Your medical writers and safety reviewers select which documents take part, and how samples are handled is agreed before the evaluation starts.
Ask for the compliance pack to see how location, access and custody are set out, before you release any trial data.
Your medical writers and safety reviewers grade the output on documents you choose. If it does not meet their criteria, nothing changes.
Run your workload on capacity from Azita’s installations. Scope the workload and data requirements.
Discuss your workload on the fleetScope the room and workload together. Azita designs, installs and commissions the deployment.
Discuss an installation in your buildingWhere the work runs, which models are used, who has access and how long anything is kept are agreed in your proposal before any work starts. For how location, access and custody are set out, ask for the compliance pack.
Agree a representative job and the acceptance criteria. Compare the output, turnaround, data requirements and total cost before deciding.
Available to evaluate on your own workload.
On the Azita fleet, or on an installation in your building.
We'll review what you need to run and contact you to discuss the right setup.
There is no price list. Your proposal states what is being quoted, the commitment and what is included. Human review, software licences and integration are listed wherever they apply.
Add what you pay for today. It travels with your enquiry as a note, so the comparison starts from the same work.
Prefer to read first? How pricing works
On an installation in your own building, the work runs in a room of that building. On the Azita fleet, it runs in a building named in your agreement. Where the work may run is set in your agreement before any work starts.
How location, access and custody are set out for an Azita deployment, written for your auditors to review. Ask for it before you release any trial data.
Your medical writers and safety reviewers grade the output on documents you choose to release, against criteria they set. If it does not meet them, nothing changes.
The cases, where they are processed and how they are handled are agreed before the evaluation starts. You choose what to release.
Proposal based on your workload and deployment. It states what is being quoted, the commitment and what is included, and lists human review, software licences and integration wherever they apply. There is no price list. An installation in your own building is its own agreement, separate from hosting capacity for others.
Exit, removal and how trial data is handled at the end are set out in your agreement before you sign.
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Regulated sectors
AI for data your rules keep on your premises, with the compliance pack first.
The page for every kind of work in this group, and how an evaluation works.
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Tell us your sector, where the data must stay and what your auditors need to see. We agree a representative job and how samples are handled before the evaluation starts.
Arrange a workload evaluation