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PharmaDiagrams - Free PFD Editor for Pharma Manufacturing

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You already know this workflow is broken.

The PFD is in Visio. The parameters are in Excel. The version everyone reviews is a PowerPoint.
When one step changes, you update everything by hand, hoping nothing drifts out of sync.
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Custom Data Schemas

Define your own table structures — not just our defaults. Track whatever your process needs.

Data LayerDocuments

Perform area clearance as per SOP.

Verify membrane integrity test (pre-use).

Equilibrate system per operating procedure.

Data LayerRelease NotesChangelog

Table:Documents

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Add ColumnNew Row

#

Description

Doc #

Owner

Verified

1

Perform area clearance as per SOP.

SOP-12435

Jessica Brown

2

Verify membrane integrity test (pre-use).

SOP-12490

Jessica Brown

3

Equilibrate system per operating procedure.

SOP-12442

Marco Silva

New row

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Resolved

Reopen

Jessica Brown2d ago

TMP upper limit should be 1.5 bar per membrane supplier specs. The diagram still shows 2.0 bar from the old Pellicon 2 cassettes — we switched to Pellicon 3 last quarter.

Marco Silva1d ago

Confirmed with vendor docs. Updated in PS-003 and PS-004.

Jessica Brown marked as resolved18h ago

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Need GxP compliance? We're ready when you are.

The free editor is everything you need to build your PFDs. But when your work requires validation, PharmaDiagrams Enterprise adds what regulators expect: formal approval workflows with sign-off, complete audit trail, electronic signatures compliant with 21 CFR Part 11, and a full IQ/OQ/PQ documentation package.

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Approval Workflow

In Progress

Document:UFDF-001-R03·Ultrafiltration/Diafiltration Process

Signature Progress2 of 3 signatures

Dr. Sarah ChenProcess Engineer

Meaning:Authored

Signed electronically

Feb 7, 2026 · 09:14 AM

Marco SilvaQA Specialist

Meaning:Reviewed

Signed electronically

Feb 7, 2026 · 02:47 PM

3

Elena RodriguezQA Manager

Meaning:Approved

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21 CFR Part 11 Compliant·All signatures include timestamp, user ID, and meaning

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