APIsIntermediatesImpurity standardsPellets
Purity,
plotted.
APIs and intermediates out of Mumbai. Every batch ships with its chromatogram, its certificate of analysis and the papers your QA team will ask for next.
Sample figures. Every number on this page is demo data except CAS numbers, formulas and molecular weights.
§00Foundations
Colours taken off the warehouse floor.
Bench-white paper on a lab-notebook grid, graphite ink and one safety orange. Status colours are the GMP labels already stuck on every drum: quarantine yellow, released green, rejected red.
Archivo · width 62–125Display
AaAaAa
One family, three widths. Condensed for dense labels, regular for headlines, expanded for stencil-like caps.
Geist 400Reading
Contains not less than 98.0 per cent.
Quiet and even, so specifications and definitions read like a pharmacopoeia, not an advert.
Geist MonoData
144701-48-4
CAS numbers, batch codes, retention times, dates. Anything a QA team copies into a system.
Documents lose one corner, like a cut label. Only CoAs and records get it.
Ink rule opens a section, grey rule splits rows, dotted rule leads to a value.
Ticks every 12 px, long tick every 60 px. Section heads sit on a ruler.
Lines draw in on one measured curve. Nothing bounces.
§01CAS lookup & register
Type a CAS number. The checksum answers back.
The last digit of every CAS number is a check digit. The field does the arithmetic as you type, so a transposed digit is caught before it becomes a wrong quote.
§02Monograph
A product page that reads like a pharmacopoeia.
Structure drawn from its SMILES string, identity line, definition, grades, tests and filings, in the order a regulatory reviewer reads them. Pick a molecule from the index or the register.
§03Certificate of analysis
The CoA, live, with its warehouse status on top.
Switch batches to see the same document in three states: released and signed, under test with results still coming in, and in quarantine before sampling.
§04Dossier builder
Ask for exactly the CTD sections you need.
Module 3.2.S, section by section. The open part comes to you; the restricted part goes to the agency under a letter of access. Both are marked before you ask.
§05Enquiry record
The RFQ form, laid out like a batch record.
Numbered entries, a graduated cylinder for quantity, tick boxes for grades and papers, and a signature to submit. Once signed the record locks and writes an audit trail.
§06Stability study
Shelf life, shown as data, not a claim.
ICH long-term and accelerated conditions on one chart, with the specification band behind them. Hover or drag across to read every pull point.
§07Shipment logger
Twenty-four days at sea, read off the data logger.
The temperature trace from inside the container, against the 15–25 °C label claim. Mean kinetic temperature is worked out from the readings, and the one excursion is marked where it happened.
PO-2611 · Telmisartan · 40 × 25 kg · Logger TL-0482
§08Reaction windows
What the plant can run, on one temperature axis.
Every reaction class as a bar from its lowest to its highest working temperature. Select one to see the vessels in the fleet that can run it, drawn to scale.
§09Market ledger
Which molecule can ship to which market today.
Agencies across, molecules down, GMP-style tags in the cells. Pick an agency to sort the ledger by what is filed there.
Filing status is sample data.
§10Audits & certificates
An audit trail you can scroll, and paper with an expiry.
Inspections and customer audits as a dated ledger with their outcome. Certificates show the time left on a graduated bar, so a renewal is visible months ahead.
Audits, certificates and dates are sample data.