All applications583

Find your application

583 applications

Open full catalog

Browse applications by category or open the full catalog.

ERP for Pharma · Available now

Follow each batch from incoming material to reviewed release.

ERP for Pharma connects material purchasing, production and financial records with batch release reviews and stability studies. Products, bill of materials and Routings define what is made; Lots retain supplier, production and expiry context.

  • No per-user fees
  • Manual work is free
  • Configure it in Proto
OverviewLot status and expiry
Pharma ERP · Lots

Lot status and expiry

Lots in one list

New lot
Lots in view
6
Total quantity on hand
2,300
Available
2
Quarantine
2
Available2
ZC-26-0814Electrolyte sachets, 10 pack
370
15 Oct
SO-26-0719Electrolyte sachets, 10 pack
100
09 Oct
Add
Quarantine2
AB-26-0930Vitamin D drops, 400 IU, 30 ml
460
20 Oct
CB-26-1103Cough syrup, 100 ml
330
21 Oct
Add
Expired1
BF-26-1022Zinc tablets, 25 mg, 60 count
910
18 Oct
Add
On hold1
CR-26-0828Zinc tablets, 25 mg, 60 count
130
16 Oct
Add
ZC-26-0814Lots · LTS-16403
Available
Lot numberL26-1662
ProductElectrolyte sachets, 10 pack
Received date15 Oct
Expiry date17 Oct
Quantity on hand370
Purchase approvalLTS-16403 · ZC-26-0814

Approver reviews the commitment independently of Buyer under the agreed spending policy.

Waiting for Approver
ApproveReturn
Example screen with sample data
Tables, ready to use
70
Saved views
16
Roles with set permissions
9
Reports and dashboards
9
Features

Review batches and operating exceptions

Every feature works on the same records. Pick one to see the screen your team works in.

Batch release and stability

Connect batch review decisions with certificate, expiry and stability evidence.

  • Review ownership
  • Decision progress
  • Stability evidence
  • Batch release reviews
  • Stability studies
  • Lots
  • People
  • Users
  • Certificates
Explore batch release and stability
OverviewPending batch release reviews
Pharma ERP · Batch release and stability

Pending batch release reviews

Approval conditions

New
BatchQA reviewerCertificate numberExpiry dateStatus
Cough syrup, lot CS26106Owen HartBRR-7071816 OctPending
Zinc tablets, lot ZT26102Mei TanBRR-5462025 OctPending
Antacid tablets, lot AT26104Luis MorenoBRR-7536122 OctPending
Zinc tablets, lot ZT26102Mei TanBRR-2335418 OctPending
Barrier cream, lot BC26108Sanjay PatelBRR-9695103 NovPending
6 of 6 records
Cough syrup, lot CS26106Batch release reviews · BRR-70718
Pending
QA reviewerOwen Hart
Expiry date16 Oct
Example screen with sample data
Process

From demand to reviewed batch delivery

From demand to reviewed batch delivery ships ready to use. 2 steps need a named approval before the work moves on: Purchase approval (Approver) and Batch release approval (Industry Reviewer).

Drag a card to another stage, or focus it and use the arrow keys. It updates to match the stage.

  1. Demand and release

    Review customer demand and supply proposals before releasing production against the selected bill and route.

    ZC-26-0814LTS-16403 · Production Planner
    Demand and releaseBy Production Planner
  2. Purchase approval

    Have Approver review the purchasing commitment independently of its preparer.

    ZC-26-0814LTS-16403 · Approver
    Purchase approvalBy Approver
    ApprovalApprover reviews the commitment independently of Buyer under the agreed spending policy.
  3. Receive and inspect

    Record incoming material and the required inspection disposition before it becomes usable stock.

    ZC-26-0814LTS-16403 · Quality Inspector
    Receive and inspectBy Quality Inspector
  4. Produce accepted output

    Receive previously unreceived accepted terminal output with required quality decisions resolved.

    ZC-26-0814LTS-16403 · Shop Floor Supervisor
    Produce accepted outputBy Shop Floor Supervisor
  5. Batch release approval

    Bring batch, reviewer, certificate and expiry evidence to Industry Reviewer before the release decision.

    ZC-26-0814LTS-16403 · Industry Reviewer
    Batch release approvalBy Industry Reviewer
    ApprovalIndustry Reviewer examines the attributed batch evidence and approves release after the required review.
  6. Ship and reconcile

    Record eligible delivery once and reconcile its invoice and financial effects within the accounting period.

    ZC-26-0814LTS-16403 · Accountant
    Ship and reconcileBy Accountant
Inside a record

Connect batch evidence with production and finance

Open any lot to see its batch release reviews, the roles that work on it, its process stages and its approvals on one page.

  1. 1
    Record details

    Lot number, Product, Received date and Expiry date.

  2. 2
    Batch release reviews

    Each line is linked to this lot.

  3. 3
    Who works on it

    Industry Reviewer and Industry Specialist, each with their own permissions.

  4. 4
    Process stages

    Execute production, with the role that acts.

  5. 5
    Approvals

    Purchase approval and Batch release approval, with who decides.

Lot status and expiryZC-26-0814
Pharma ERP · Lots

ZC-26-0814

Electrolyte sachets, 10 pack · Available

Log activity
1
Record details
Lot numberL26-1662
ProductElectrolyte sachets, 10 pack
Received date15 Oct
Expiry date17 Oct
2
Batch release reviews

ZC-26-0814

BatchQA reviewerCertificate number
Cough syrup, lot CS26106Owen HartBRR-70718
Zinc tablets, lot ZT26102Mei TanBRR-54620
Antacid tablets, lot AT26104Luis MorenoBRR-75361
Batch release reviews
6
3

Who works on it

  • Industry ReviewerView batch release reviews, Lots, People, stability studies
  • Industry SpecialistManage stability studies
4

Process stages

  • Execute productionShop Floor Supervisor, Operator
5

Approvals

  • Purchase approvalApprover
    Approved
  • Batch release approvalIndustry Reviewer
    Waiting
Example screen with sample data
Approvals

Keep purchasing and batch decisions accountable

OverviewApprovals
Pharma ERP · Overview

Approvals

Signed in as Approver

Waiting for you

4 To review1 Overdue2 Decided todayOnly mine
0 selectedApproveReturn
  • PO-37345$18,420.00
    Northbank Bottle WorksRequested by Fatima Okafor
    Submitted1dActions
  • PO-17280$7,890.00
    Harborline Closure Co.Requested by Mei Tan
    Submitted2dActions
  • PO-97873$12,350.00
    Willow Chemical SupplyRequested by Owen Hart
    Submitted5dActions
  • PO-57558$5,640.00
    Cedar Grove IngredientsRequested by Owen Hart
    Submitted6dActions

Who approves what

DecisionApprover
Purchase approvalHave Approver review the purchasing commitment independently of its preparer.Approver
Batch release approvalBring batch, reviewer, certificate and expiry evidence to Industry Reviewer before the release decision.Industry Reviewer
2 approval rules · set per role in Proto
Example screen with sample data
Roles

A workspace for each role

Everyone opens Pharma ERP to the work that is theirs. Pick a role to see what it starts with.

Production Planner

Owns MRP, work-order release, scheduling, and BOM/Routing maintenance.

This is the first screen this role sees.

OverviewProduction schedule

Production schedule

Work order operations · Production Planner

Work orderOperation numberWork centerOperatorPlanned startPlanned end
Vitamin D drops 400 IU, batch 2610370Cream mixing vessel 2Marco Bellini26 Oct01 Nov
Electrolyte sachets, batch 2610510Liquid filling line 2Elena Voss19 Oct26 Oct
Electrolyte sachets, batch 2610530Powder blending room 3Nadia Karim27 Oct30 Oct
Oral saline 500 ml, batch 2610150Powder blending room 3Owen Hart18 Oct21 Oct
Skin barrier cream 50 g, batch 2610870Powder blending room 3Fatima Okafor24 Oct30 Oct
6 of 6 records
Example screen with sample data
Reports

Follow expiry, quality work and financial exceptions

Review batch evidence, stock exposure, production output and financial exceptions.

Overview
Pharma ERP · Overview

Pharma ERP dashboard

This quarter

Work order operations in view
6
Pending
3
In progress
2
On hold
1

Lots by status

How far records got this quarter

StageReachedStep
Available28
Quarantine1864%
On hold1056%
Consumed770%

Quantity on hand by status

Sample totals per stage

10.0k0
10.0kAvailable
6.0kQuarantine
8.0kOn hold
5.0kConsumed
8.0kExpired
Example screen with sample data
  1. 01Batch release decisions

    Which batches remain Pending or Testing, who is attributed as reviewer, and which certificate or expiry evidence needs examination?

  2. 02Stability follow-up

    Which dated pulls remain Pending or Investigate, and what result is retained for the batch and storage condition?

  3. 03Lot expiry exposure

    Which current lot quantities are available, held or expired, and which expiry dates fall within the review window?

  4. 04Open quality actions

    Which corrective work is overdue or Completed without independent verification?

  5. 05Material availability

    How does on-hand stock compare with allocated quantity and the dated reservations that require it?

  6. 06Supplier invoice differences

    Which invoice exceptions remain unresolved, how do invoiced and expected values differ, and who owns investigation?

  7. 07Production interval output

    How much good and scrapped output was reported within completed production-log intervals for a work order or work center?

  8. 08Period posting review

    Which dated entries remain Draft, and how do posted debit and credit lines reconcile within the accounting period?

  9. 09Standard cost elements

    Which effective version carries the current material, labor, overhead and outside-processing values for the product?

Controls

Review holds and repeated-event handling

Each stage, from demand to reviewed batch delivery, names the role that acts and the status it records, so a change is never anonymous.

OverviewFrom demand to reviewed batch delivery
Pharma ERP · Process

From demand to reviewed batch delivery

Each stage, the role that acts and the status it records

Process stages
12
Approval steps
2
Roles involved
9
Tables touched
37
Master data and policyApproval
Production Planner, Accountant, Approver, Buyer
StatusDraft → Active
RecordsEngineering change orders, Bill of materials, Chart of accounts
Demand and release
Production Planner
StatusProposed → Firm → Released
RecordsSales order lines, Planned orders, Sales orders
Purchase approvalApproval
Approver, Buyer
StatusDraft → Submitted → Approved
RecordsPurchase orders, Requisitions, Approvals
From demand to reviewed batch delivery
  1. Start
    Master data and policyDraft → Active
    Engineering change orders
  2. Step
    Demand and releaseProposed → Firm → Released
    Sales order lines
  3. Approval
    Purchase approvalDraft → Submitted → Approved
    Purchase orders
  4. Step
    Receive and inspectPending → pending QC → Accepted
    Quality inspections
  5. Approval
    Match and authorize paymentMatched → Approved → Scheduled → Paid
    Supplier invoices
Example screen with sample data
AI agent

Prepare evidence and exceptions with Proto

Prepare batch evidence and operational exceptions while preserving human decisions.

It can

  • Industry Reviewer: Show Pending and Testing batch reviews with their batch, quality reviewer, certificate number and expiry evidence; identify mismatches for the reviewer to examine.
  • Industry Specialist: List stability pulls due by today, keeping storage condition, result and disposition with the linked batch.
  • Production Planner: Compare the selected work order's bill and route with its component and operation records, then list shortage evidence requiring owner review.
  • Quality Inspector: Find Completed corrective actions that still need independent verification and retain the original owner and finding context.

Stays with a person

  • A human approval must use the authorized person's verified decision route.
  • Agree the decision route with Industry Reviewer and Approver, and test the actor used for floor recording with Shop Floor Supervisor.
  • A recommendation cannot approve a batch, waive a hold or reopen a locked period on its own.
  • Use the actual actor and source identity for capture and replay controls.
Integrations

Connects to the tools you use

Set up connections through ERP.AI and Proto workflows, with every change logged.

  • Pharma ERP
  • Laboratory and document systems
  • Supplier exchange
  • Shop-floor scanners and instruments
  • Carrier service
  • Bank and external ledger
Data model

Your data, in tables you can change

Every record lives in a table you can see, extend and export. Add fields or whole tables in Proto.

Browse all 70 tables
70tables
  • Batch release and stability6
  • Product engineering11
  • Demand and production15
  • Purchasing and receiving14
  • Inventory and traceability12
  • Quality10
  • Costing and finance14
Implementation

Roll out one team at a time

Start with one team and one process, then add the rest once the basics are running.

  1. Agree the operating scope

    Select a product, incoming supplier lot and production order the operations and quality owners can review together. Include its batch release and stability follow-up. Keep external laboratory execution, signatures and regulatory submissions within their separately agreed systems.

  2. Map reference data

    Reconcile products and supplier-to-vendor identity, then the selected bill and route. Map the specialty reviewer to their user account and verify the employee mapping used by assigned-work and purchase views. Import lot and certificate evidence with original identifiers and dates.

  3. Configure views and controlled routes

    Set up the operating views and reports with their named owners. Agree the controlled purchasing and batch decision routes and test them with the reviewer accounts. Confirm who can perform floor commands and who records the resulting production evidence.

  4. Rehearse physical and quality controls

    Attempt issue from an expired or held lot, a duplicate receipt and a repeated accepted completion. Try an inspection with an overdue instrument and self-verification of corrective work. Each rejected command must leave its affected quantity and financial result unchanged.

  5. Review specialty evidence

    Capture the pilot batch review with the correct quality reviewer and certificate context. Reject repeated evidence identities. Rehearse a stability correction through the attributed successor-evidence route; review the original and successor evidence together before accepting the correction.

Pricing

$0per user

The base account and everyday work in the ERP.AI app are free, for every user.

  • No per-user or per-seat fees
  • Viewing, editing, approving and exporting records in the app is free
  • Pay only for machine work: API calls, imports, workflows and AI agents
  • Prepaid credits from $5. Purchased credits never expire

Pricing details

Machine work rate card Included per $1 of credit

Machine work rate card
UsagePer $1
Record reads (list, filter, get)20,000
Search or aggregate queries4,000
Record writes4,000
Imported or synced records200,000
Workflow runs2,000
AI agent runs2,000
Scheduled jobs or webhooks20,000
File uploads (MB)2,000
CSV or PDF exports100
FAQ

Questions, answered

Scope, rollout and pricing for Pharma ERP.

All questions
How do I get started?

Click Get started, then use Proto to configure ERP for Pharma for your business. Start with a reviewed product definition, an incoming supplier lot and a production order. Follow accepted output through batch review and a stability pull, then reconcile its stock and financial effects before expanding.

What does the Batch Release Reviews screen show?

The Batch Release Reviews screen presents a batch release review queue, status distribution, certificate and expiry evidence, and selected-record review history. The batch release review links the review to lots and quality reviewer in the person record. Confirm the reviewer account mapping and controlled decision route during setup.

Does an Approved batch review replace the quality hold decision?

The batch review status records the specialty decision. The quality hold retains its own disposition and release attribution. Rehearse the operating controls that connect eligible production and shipment to required quality decisions; review both decisions before treating the material as usable.

How are stability pulls recorded?

Each stability study records batch, storage condition, pull date, result and disposition. Pending, Accept and Investigate separate the evidence states. Configure the correction route to retain original evidence and attributed successors, then reject repeated capture of the same source evidence.

Can reviewers approve just because they can open the queue?

Separate evidence preparation from the human decision. Agree the permitted approval route with Industry Reviewer and Approver, then rehearse it using their actual accounts. The preparer must be refused if they attempt to approve their own purchasing commitment.

How is expiry handled during material issue?

Each lot carries expiry date and status. Require lot-controlled issue to use an Available, unexpired lot of the intended product. Rehearse the expiry boundary and unresolved holds against actual movement commands before relying on the control.

Where do laboratory results and controlled documents come from?

Use the lab's approved result records and the controlled-document system agreed with your quality owner. Map each result to the correct batch, retain its actual evidence date and review corrections against the original. Agree provider access and the acceptance checks before enabling the connection.

Can we connect laboratory, scanner or carrier systems?

Connections require explicit configuration, provider access and source mappings. Agree the source owner and permitted operating command for each feed. Rehearse duplicate events, wrong references and external failures before enabling a feed; see integrations.

How do we avoid duplicate inventory and accounting effects?

Bind each receipt, completion, shipment and material posting to its actual source identity so retries return the original effect. Test repeated commands and conflicting content during implementation. Batch review and stability capture must not create another physical or financial effect.

What does implementation and ongoing use cost?

Use the pricing page for the published policy. Agree implementation scope after reviewing your reference mappings, approval routes and required connections. The implementation plan sets out the pilot evidence to review before wider cutover.

Set up Pharma ERP your way.

Start free, then use Proto to change fields, steps and approvals before your team goes live.

How to get started

A personal agent for your business

Get started with Proto

Your app is selected. Download Proto, then open it with this context.

Selected appERP for Pharma

Choose your computer’s platform.

Download Proto

Install Proto, then return to this panel.

Already installed? Open Proto

Free to use. Your own model provider may charge for usage.