noxVIEW
Pharmaceutical
Industry Solution

Pharmaceutical

FDA & GMP Compliant Manufacturing Solutions

Purpose-built solutions for pharmaceutical manufacturers — from batch manufacturing records to environmental monitoring, ensuring quality and compliance at every step.

Industry Challenges

1
Strict FDA 21 CFR Part 11 and EU Annex 11 compliance requirements
2
Complex batch manufacturing with multi-step recipes
3
Environmental monitoring for cleanrooms and controlled areas
4
Material traceability from raw material to finished product
5
Long audit trails and data integrity requirements
6
Manual documentation causing delays in batch release

Our Solutions

Electronic Batch Records

Paperless BMR with digital signatures, automated deviation detection, and review-by-exception for faster batch release.

Environmental Monitoring

Real-time monitoring of temperature, humidity, particle counts, and differential pressure across cleanrooms.

Equipment Qualification

IQ/OQ/PQ documentation management with automated protocol execution and report generation.

Quality Management

Integrated QMS with CAPA, deviation, change control, and OOS investigation workflows.

Lab Integration

LIMS integration for seamless QC testing, CoA generation, and stability study management.

Serialization

Track & trace compliance with aggregation, commissioning, and regulatory reporting.

Ready to Transform Pharmaceutical?

Discover how noxVIEW can address your specific industry challenges.

Book a Demo