Manufacturing · Compounding · Distribution
Records that outlive the people who made them.
Exposure records are kept for thirty years. That is not a policy you write down. It is a control you either have or you do not.
What ASIP saves you
Saves time
The exposure record, the safety data sheet and the containment check are one chain. Tracing one exposure does not take a fortnight.
Saves money
One platform across EHS and exposure monitoring. No separate archive product to hold what you are legally required to keep.
Saves effort
The audit trail is append-only and nothing can be edited after the fact. There is no reconciliation to do, because there is nothing to reconcile.
Catches it earlier
Exposure trends by task and area are visible while they are still trends, not after a monitoring result comes back.
What you get on day one
- Exposure records with enforced long-term retention
- Chemical inventory and safety data sheets
- Deviation, investigation and CAPA
- Containment and PPE programme records
- Risk assessment by task and area
- Append-only audit trails on every record
- OSHA 300 log across every site
Everyone says AI. Here is ours.
Four things it does, and one thing it is never allowed to do.
- Two models, not one
- One drafts. A second, different model checks it before you see it. A model marking its own homework is the weakest possible safeguard.
- It cites, or it stops
- Answers come from your own documents and name the source. No source, no answer — it says so rather than inventing something that sounds right.
- You can argue with the score
- Expected against observed, with every input listed. Not a number between one and a hundred that nobody on your team could defend to an auditor.
- A person always decides
- It never closes an action, decides recordability, or signs anything off. It drafts. You decide.
Where the line is
Retention is not a promise in a policy document. Deletion is blocked by a database trigger, and the period is configuration you can inspect. Where 29 CFR 1910.1020 applies, that is thirty years. ASIP is not a QMS or a LIMS and makes no 21 CFR Part 11 validation claim.
You can see the price before you call us.
Every other platform in this market makes you book a demo to find out what it costs. Our calculator returns your figure from your headcount, your sites and your industry. Every module that applies to pharmaceutical is included, there is no per-user fee, and onboarding, data migration and support are part of the number.