Rx

PharmaGPT

Pharmaceutical Validation Platform

Overview
Gemini 2.5 Flash  ·  Online

Welcome, back

Your Workspaces

Executive Workspace

Dashboards, KPIs, Executive Insights

Validation Workspace

Validation Projects & Qualification

Quality Workspace

CAPA, Deviations, Change Control

Knowledge Workspace

SOPs, Manuals & Reference Documents

Document Workspace

Controlled Document Authoring

PharmaPilot

Enterprise AI Assistant (placeholder only)

Home Dashboard

Everything that needs your attention, at a glance

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Projects
Across all active work
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Validation Projects
In the Validation Workspace
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Knowledge Base Docs
In the document library
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Protocols Generated
Via the document generator
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Pending CAPAs
Awaiting closure
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Pending Deviations
Requiring investigation
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Avg Validation Score
This session
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Equipment
In the equipment library
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Controlled Documents
Due for review
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Change Controls
Pending approval
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Validation Status
Awaiting review or approval
Quick Actions
Recent Activity
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Recent Projects
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Upcoming Reviews
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Recent AI Conversations
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System Health
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Validation Dashboard

Validation Suite — company-wide status at a glance

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Active Projects
Across the Validation Suite
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Open URS
Draft or under review
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Qualification Progress
IQ / OQ / PQ completed
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Pending Approvals
Across all suites
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Validation Reports
Total on file
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Equipment Count
In the Equipment Library
Recent Projects
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Quality Summary
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Approval Queue
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My Pending Approvals
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Recent Activity
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PharmaPilot

Enterprise AI Assistant — coming soon.

This workspace is a placeholder for a future phase. Use AI Assistant below for the current chat assistant.

PharmaGPT is your AI-powered pharmaceutical consultant with 30+ years of simulated expertise. Select or create a Project in the sidebar, then ask about GMP compliance, validation protocols, CAPA, regulatory submissions, or any pharmaceutical engineering topic.

Press Enter to send  ·  Shift + Enter for a new line

Project

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Select a project to manage its equipment.

Equipment Records

No equipment recorded yet.

Add your first Equipment record using the button above.

Select a project to view its Document Insights.

Select a project to manage its documents.

Drag & drop a file here

PDF, DOCX, XLSX, TXT  ·  Max 50 MB

Uploaded Files

No documents uploaded yet.

Upload your first file using the area above.

Risk Assessment

Open the Risk Management Suite. Not yet filtered to this project — see Known Issues.

URS

Open the URS Management Suite. Not yet filtered to this project — see Known Issues.

Qualification

Open the Qualification (IQ/OQ/PQ) Suite. Not yet filtered to this project — see Known Issues.

Validation Report

Open the Validation Report Suite. Not yet filtered to this project — see Known Issues.

Tasks
Planned
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Equipment

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Knowledge Base

Permanent document library — SOPs, protocols, regulations & more

Folders
Documents

Equipment Library

Every Equipment record across every project — company-wide

Equipment Records

No equipment recorded yet.

Equipment is added from inside a project's own Equipment tab.

Company Administration

Create companies and their first Company Admin — Super Admin only

User Management

Users in your company

Department Management

Departments and designations for your company

Departments

Designations

Roles & Permissions

Manage roles, the permission matrix, user assignments, and the audit trail

OQ

Operational Qualification

OQ — Protocol Generator

No project selected
Equipment
Details
Documents
Generate

Risk Management

ICH Q9 · GAMP 5 · EU GMP Annex 15 · WHO-GMP · 21 CFR · ISO 14971

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Risk Assessments

Create, manage, and review pharmaceutical risk assessments

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Risk Library

Reusable risk database — enriched from approved assessments

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Templates

Pre-built risk assessment templates for common pharmaceutical activities

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Risk Reports

Generate and export professional GMP-compliant risk reports

Select an Assessment

Open an assessment and click "Report" to generate a risk report here.

Workflow Inbox

Every pending Workflow Engine approval assigned to you, across every module

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Review & Approval

Assessment review workflow, approval trail, and status management

Select an Assessment to Review

Open an assessment from the list and click "Review" to manage approvals.

AI Risk Assistant

Expert pharmaceutical risk management guidance powered by Gemini 2.5 Flash

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URS Management Suite

GAMP 5 · ASTM E2500 · EU GMP Annex 15 · 21 CFR Part 11 · WHO GMP · ICH Q9/Q10

URS Documents

All User Requirement Specifications

New User Requirement Specification

Create a GMP-compliant URS with AI-assisted requirement generation

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Category
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Project Info
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Generate
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Requirements
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Complete
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Draft

Qualification Management Suite

IQ / OQ / PQ Protocol Management · EU GMP Annex 15 · GAMP 5 · 21 CFR Part 211

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Validation Report Management Suite
EU GMP Annex 15 · GAMP 5 · 21 CFR Part 11 · WHO GMP · ICH Q9

All Validation Reports

GMP-compliant Validation Report lifecycle management

Report # Title / Equipment Department Status Type Completeness AI Score Created
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