Make writing records
a pleasure
Every industry gets an interface designed for it.
Built for records
linked to testing and inventory
Not a Word-style set of input boxes: experiment records, sample numbering, testing progress, report delivery, review workflow and inventory are all integrated in the ELN.
01Structures & reactions
An industry first: chemical structures are drawn automatically and the stoichiometry comes with them — no calculator needed.
02Audits made easy
Every number is controlled and written into the audit trail, from sample IDs through to completed signatures, so the whole process is fully traceable.
03TLC annotation
The system marks Rf values on the TLC automatically, and structures can be labelled on each spot. An hour of work now takes a minute.
04Photo & video management
Images or video can be attached at any step of the procedure for easy reading, and chemical structures can be annotated on the images.
05Sample submission
For third-party testing, R&D and production units, the ELN and the sample platform are fully integrated. There is no need to buy several systems separately to get seamless, efficient collaboration.
06Automatic stock deduction
The ELN links to inventory: materials are deducted automatically during the experiment, so stocktaking is simple. Expired materials are kept out of your hands, and the opening date is recorded automatically, which keeps ISO 17025 audits straightforward.
Suitable for every industry:
R&D, testing, production, QC and QA
Templates and departments are enabled by your subscribed industry; new templates are continually being developed.
Every record is evidence by design
Click a status to see what is controlled at each stage.
From the moment an ELN draft is created it is protected by SHA-256 control, with the full edit history preserved and multi-user editing supported. Even unpublished drafts cannot be deleted at any permission level, protecting data authenticity and integrity to the highest security standard.
The system supports cyclical review: every step, whether submit, approve, return, withdraw or void, is written precisely and irreversibly to the audit trail, keeping the review chain transparent and traceable.
Handwritten-image encrypted e-signatures with recorded review reasons help labs clear regulatory hurdles. Aligned with FDA 21 CFR Part 11 §11.50 and §11.70, any change after approval is strictly monitored and logged, and tamper-evident PDF reports build an unbreakable chain of trust for your research assets.
Once signing is complete the record is released and locked, and its content can no longer be edited. The released PDF carries a verification code for outside parties to check; any later change is handled as a new version, with the original record kept intact.