What sets us apart
Value for the plant at the fastest pace, without stopping production or waiting for a vendor.
10X value for Manufacturing, Quality and IT
A rollout usually costs three leaders the most: production time, control, and servers and projects. The levers stay with the people who run the plant.
Value without touching the production schedule
- Training at their own pace, on their own phone or tablet, between shifts
- Screens they already know: built from your own BMR, in its order and words
- No waiting for a vendor: study guides, manual, videos and agents, any time
- Waves and rehearsals for hundreds of people, from your own BMR
Quality built into every step
- Limits checked as values are entered; a deviation before the signature
- People certified, booths cleaned, equipment calibrated, before anyone signs
- An approved BMR to another area the same day, under change control
- Records you can defend: Part 11 signatures, a full audit trail, nothing deleted
Less to run, control kept
- Nothing to install, patch or back up in the plant
- Upgrades without projects: each release qualified, checked on each site
- Access you control: roles, two-step sign-in, each company's records apart
- Three sites: development, QA with OQ and PQ, production
Four products, one platform
Take them together, or start with any one. The eBMR, eLogbooks and QMS share the plant's equipment, people and signatures; the Auditor checks the records of the systems you already have.
Atto Pharma eBMR
Batch manufacturing and packing records from your own approved Word or PDF BMRs, filled in on any browser, tablet or phone.
- Screens generated from your BMR: every entry, limit and signature, in its order; a revision is a new version, compared and approved
- One BMR, every process area: extended in a guided draft, equipment matched, each changed limit with its reason
- On the floor: dispensing, equipment and cleaning, deviations at the field, review and release, the executed record as a PDF
- Training built in: a path per role, study guides, exams in Telugu, Hindi and Tamil, certificates, waves and rehearsals
- An agent for every role: answers from your manual and SOPs; agents on your records answer QA and production with charts
Work in progress: where every open batch is, by operation, with the record's sections on the left. Made-up data.Atto eLogbooks
Equipment, utilities, HVAC, maintenance, calibration, area and laboratory logbooks as electronic records, with the same rules as the batch records.
- 40 ready templates: utilities, HVAC filters, preventive maintenance, instrument calibration, breakdowns, area temperature and humidity, registers, microbiology
- About a minute to the first reading: pick, adjust in a few clicks, QA approves with the password, issue, record
- Trends drawn automatically for every reading with a limit; calibration results worked out as typed
- Your own forms too: loaded from Word or PDF and converted into templates you check
A logbook's trend: ten days of a dispensing booth's humidity against its limit, the excursion in red. Made-up data.Atto QMS
Change control, out-of-specification results and CAPA as electronic records, on their own or with the eBMR and eLogbooks. Every step in its turn, by the right person, signed with the password.
- Change control: the initiator, the head of department, QA, the departments that concur and the QA Head; the impact checklist, the actions, closure and the effectiveness check
- OOS results: Phase IA and IB in the laboratory, the hypothesis plan, retests by a second analyst, Phase II and III, the disposition by the QA Head
- CAPA: the actions with their owners and due dates, verified by QA, then the effectiveness check
- Checked by the database: the order of the steps, a second person, timelines and extensions, nothing closed while an action is open; an audit trail chained by hashes
- With the eBMR: an open OOS on a batch holds its QA release until the OOS is closed
- Raisedby anyone with a QMS role, in their own department
- Reviewedby the head of department and QA
- Approvedby the QA Head, as major or minor
- Done and verifiedeach action by its owner, checked by QA
- Closed and checkedclosure, then the effectiveness check
Atto Auditor
Your MES, QMS, LIMS, training, document and logbook systems each tell their own truth. The Auditor reads their exports, compares the records the way an FDA investigator would, and lists what an inspection would likely question, with the records behind each finding.
- Ranked by what FDA cites: each problem with how often it appears in FDA's recent warning letters to drug manufacturers
- Works with the systems you have: CSV and Excel exports and reports, recognised from their column names; you confirm the columns once
- Your records stay with you: the audit runs in your own browser; the files are not uploaded, and no AI model reads them
- Per plant: a free trial for all your plants, then a monthly price per plant, 20% off from 10 plants and 50% off from 30
- Inside Atto Pharma eBMR, QMS and eLogbooks too: Audit → Atto Auditor, with the same sign-in
- Exportfrom your MES or eBMR, QMS, LIMS, training and logbook systems
- Choosethe files in your browser: nothing is uploaded
- Comparedrecord against record, across the systems
- Findingsranked by how often FDA cites them, each with its records
- Before the inspectionfix the gaps and run it again
From your approved BMR to go-live
Each step is done by your own team, on your own timeline.
Read more
One-page brochures to share with your team, whitepapers for a deeper look, and the blog.
All whitepapers, including Electronic Logbooks in a Minute →
Compliance by design
See your own BMR on screen in the 14-day pilot
Sign up your company on the evaluation site, load a BMR, and see its screens the same day. No installation, no implementation project.
How we sell
Siddhi LLC is a software company based in San Jose, California. The manufacturing products are subscriptions per user per month, billed annually or half-yearly in advance by invoice in US dollars, payable through a secure Stripe payment page (card or US bank account, ACH) or by wire transfer. Every new company starts with a free 14-day pilot. Customers in India are invoiced in Indian rupees, with GST and applicable taxes, through our billing partner in India, Atachi Software Systems Private Limited. See Pricing, the Terms of Service and the Refund & Cancellation Policy.
Siddhi pharmacy growth platform
Connects established pharmacies with attributed demand and with stock owners who fund inventory. Pharmacies are not charged to use the platform.