GxP Platform — euGMP, GACP & GDP Compliant

Your Quality Assistant for

euGMP Compliance

Generate SOPs, Validations, Audits, HACCP, ISO, euGMP, GACP and GDP documents tailored to your facility. Manage Non-Conformances and correct them with your Quality Assistant. Guided by EMA guidelines.

No credit card required

0+
Document types
0+
Years GxP experience
0/7
Always available
0%
GxP compliant

Everything your facility needs

From SOPs to full validation protocols — BasiDocs covers every GxP requirement

📋

Quality System

Quality Manuals, SOPs, Technical Instructions, Specifications, Document Control

🔬

Validations & Qualifications

IQ, OQ, PQ protocols, Computerised Systems (CSV/GAMP5), Cleaning & Process Validation

🌿

euGMP & GACP

Full documentation for medicinal cannabis and pharmaceutical producers — GACP cultivation, euGMP processing Parts I & II, industrial pharmaceutical manufacturing

🚚

GDP Distribution

Good Distribution Practice documentation for medicinal cannabis and pharmaceuticals

⚠️

HACCP

Pharmaceutical HACCP — risk analysis, critical control points and validation for GxP facilities

📊

ISO Standards

ISO 9001, 13485, 14001, 22000 — full quality system documentation

🔍

Audits & CAPA

Audit plans, reports, corrective actions, deviation management, non-conformances

📦

Raw Materials & Suppliers

Supplier qualification, CoA management, raw material specifications

💻

Computerised Systems

CSV protocols, GAMP5, 21 CFR Part 11, audit trails, user requirements

📝

GxP Records

Production, cleaning, maintenance, training records — full traceability

⚙️

Workflows & Processes

Process flowcharts, approval workflows, version control, change control

🤝

Quality Assistant

Your 24/7 quality consultant — ask anything about GxP compliance, audits, validations

⚙️ How it works

A complete GxP platform

From the first document to a complete quality system — all integrated, traceable and compliant.

🤝
MÓDULO 1

AI Quality Assistant

The Assistant knows euGMP, GACP, GDP, GAMP5, ICH, Annex 11, 21 CFR Part 11 and all relevant ISO standards. You describe your facility — sector, certifications, equipment, processes — and it generates complete GxP documents adapted to your reality.

SOPs, ITAs, Quality Manuals adapted to your facility
IQ/OQ/PQ and CSV/GAMP5 validation protocols
GxP records, HACCP plans, material specifications
Real-time regulatory interpretation
Audit preparation for INFARMED, EMA, FDA
📋
MÓDULO 2

GxP Document Management

Document control compliant with euGMP Chapter 4 and Annex 11. Complete approval workflow: Draft → Under Review → Approved → Obsolete. Automatic versioning, review dates, full traceability.

Draft → Approved → Obsolete workflow per euGMP Ch. 4
Automatic versioning with SHA-256 hash
Word (.docx) download for authority submission
Review dates and expiring document alerts
Centralised library with type and status filters
MÓDULO 3

Deviations → Non-Conformances → CAPA

Complete quality management workflow per ICH Q10, euGMP Chapter 8 and GAMP5. When you detect a deviation or NC, the system automatically creates the corresponding CAPA with full traceability — from origin to effectiveness verification.

Deviations
Automatic codes DEV-YYYY-XXX. Categories by sector (euGMP, GACP, GDP). Critical/Major/Minor priority.
⚠️
Non-Conformances
OOS, OOT, audit findings, complaints. Direct link to audits and deviations.
🔄
CAPA
Created automatically. Root cause (5 Whys, Ishikawa, FMEA). Effectiveness verification.
🔍
Audits
Internal, supplier, regulatory, certification. Record NCs and deviations directly from the audit.
📊
MÓDULO 4

GxP Audit Trail

Immutable record of all platform actions — who did what, when. SHA-256 hash for integrity verification. PDF export with digital signature. Compliant with Annex 11 (EU), 21 CFR Part 11 (FDA) and GAMP5.

✓ Immutable record — entries cannot be altered
✓ SHA-256 hash per event
✓ GxP PDF export for inspections
✓ Compliant with Annex 11, 21 CFR Part 11, GAMP5
✓ Filter by user, date, action type

COMPLETE TRACEABILITY FLOW

AI AssistantGxP DocumentDeviation / NCCAPAAuditAudit Trail

Every action recorded with timestamp, user and SHA-256 hash

🤝 Quality Assistant

Meet your Quality Assistant

Available 24/7, with deep knowledge of EMA, GACP, GDP, ICH and all major GxP guidelines

Try for free
Ask anything about GxP compliance
Audit preparation guidance
Regulatory interpretation
Document review assistance
CAPA recommendations
Always up to date with latest guidelines
Our story

Why BasiDocs?

We know the industry from the inside. We have lived through audits, validations and regulatory submissions. BasiDocs was born from the frustration with complex, expensive and time-consuming documentation — and the certainty that it could be better.

With over 8 years of real experience in the pharmaceutical and GxP sector, we built a platform that combines specialized regulatory knowledge with cutting-edge technology — so your company always has the right documentation, at the right time.

8+Years of GxP experience
200+Document types available
100%EMA & GACP compliant
24/7Quality Assistant available
🔒 Security & Confidentiality

Your data is safe with us

Facility layouts, formulas, methods and security plans are critical information. We treat them with the utmost rigour.

🔐

AES-256 Encryption

All documents encrypted at rest and in transit. Nobody accesses your files without authorization.

🛡️

Automatic NDA

Upon registration, you automatically sign a confidentiality agreement. Your data is our secret.

🚫

Zero Advertising

Your data is never used for advertising or shared with third parties. Ever.

📋

Complete Audit Trail

Record of who accessed, changed or approved each document. Compliant with 21 CFR Part 11 and Annex 11.

🏠

Total Isolation

Each company's data is completely isolated. It is impossible to access another company's data.

🗑️

Right to Erasure

Delete all your data at any time. We fully comply with GDPR.

🔒 Your documents, facility layouts, formulas and data are stored in an encrypted and completely isolated environment. Only you have access. They are never shared, sold or used for any purpose other than the operation of your account. BasiDocs is more secure than your email.

Trusted by GxP professionals

What our customers say

5.0 / 5.0

"BasiDocs cut our SOP creation time from days to minutes. The quality is outstanding and fully aligned with EMA guidelines."

Maria S.
Quality Manager

Simple, transparent pricing

Start free. Scale as you grow.

Free

Try BasiDocs risk-free

€0
1 document generated
Word format download
Step-by-step creation guide
Basic Quality Assistant
Start Free

Starter

For small facilities

€59 /month + VAT
10 documents/month
5 updates per document
Quality Assistant (basic)
Email support
Start Starter
BEST VALUE

Growth

Best value for growing operations

€199 /month + VAT
50 documents/month
Unlimited updates
Quality Assistant (advanced)
Audit preparation support
Priority email support
Start Growth

Enterprise

For large facilities & groups

€399 /month + VAT
200 documents/month
Dedicated Quality Assistant
Platform integrations
Dedicated support
Custom onboarding
Contact us
PREMIUM

GxP Pro

Full on-site consulting & implementation

€3,500 /month + VAT
Consulting
Implementation support
Custom documentation
On-site visits

Travel & accommodation not included.

Contact us

Pay as you go

No subscription needed. Buy credits and use them whenever you need.

Buy credits
5 credits
€50 + VAT
€10/doc
POPULAR
10 credits
€90 + VAT
€9/doc
20 credits
€160 + VAT
€8/doc
🗺️ Roadmap

What we're building

Full transparency on what's done and what's coming next.

Launched
GxP document management
AI Quality Assistant 24/7
Deviations → NC → CAPA auto
Pharmaceutical HACCP (8 types)
Audits with GxP traceability
Audit Trail (Annex 11, 21 CFR Part 11)
Auto codes AUD/DEV/NC/CAPA
Dashboard with real KPIs
Affiliate system with commissions
Plans + Pay-as-you-go credits
Bilingual PT/EN
🔨In development
Staff training records
Equipment & calibration management
Automatic deadline notifications
Change Control
Create records from AI Assistant
Native mobile app
🔮Planned
Digital document signing
Multi-user per company
LIMS integration
Public API for integrations
Customer complaints module
Batch traceability
White-label for GxP consultancies
💡

What would you implement?

Have a feature idea? Tell us — the best suggestions make it into the roadmap.

Ready to simplify GxP compliance?

Join facilities already using BasiDocs. Start with 1 free document.

Start Free Today