Packaging leak tester CDV Pharma V&P

for the pharmaceutical industrylaboratorypressure

Package integrity directly affects product sterility, stability and shelf life
Leak testing methods must therefore be reliable, repeatable, and aligned with regulatory expectations. CDV Pharma V&P supports pharmaceutical laboratories and quality teams in performing consistent package integrity testing across multiple packaging formats and test methods.

A versatile leak detection system for pharmaceutical applications.
CDV Pharma V&P is a package integrity testing system designed to perform dye penetration, vacuum, and pressure-based leak tests.
Its architecture integrates:
An optimized vacuum chamber for greater packaging flexibility.
An independent control module to improves delivery times, simplifies maintenance, and protects sensitive electronics from immersion fluids.
A PLC-based automation platform.
This design ensures process stability, protection of electronics, and operational flexibility in daily laboratory use.

Multiple leak test methods. One instrument
CDV Pharma V&P supports a wide range of package integrity test methods, including:
Dye penetration testing using methylene blue
Vacuum-based leak detection
Internal pressure testing
External pressure testing for increased sensitivity
With a single system, laboratories can perform different CCIT methods depending on package type and test objectives.

Applications
CDV Pharma V&P is suitable for leak detection testing of:
Ampoules
Vials
Bottles
Blisters
Flexible and semi-flexible packages
Sealed pharmaceutical containers
Tests can be performed on rigid, semi-flexible, and flexible packages, with or without liquid content.

Designed for regulatory compliance
CDV Pharma V&P supports testing aligned with internationally recognized standards, including:
USP
USP / JP 7.03
ASTM D3078
ASTM F2096
ASTM D4991
ASTM D6653
European Pharmacopoeia 3.2.9
MGA 0486 Mexican pharmacopoeia (FEUM)
21 CFR Part 11 (optional)
This makes CDV Pharma suitable for regulated pharmaceutical quality control environments.

Data integrity and traceability
The PLC-based control system supports:
User and permission management
Automatic storage of test results
Secure PDF report generation (electronic signature optional)
Digital data export
Integration with external systems (printers, barcode and QR readers)
These capabilities support data integrity and traceability requirements in pharmaceutical laboratories.

Adapted to real production and QC environments
CDV Pharma V&P features:
Increased chamber height for greater packaging flexibility
Compact internal volume to reduce dye consumption
Independent control module for improved ergonomics and maintenance
Clear visual inspection during the entire test cycle
The modular design allows configuration changes and future upgrades.

Validate your application before investing
Send your samples and evaluate the suitability of CDV Pharma V&P for your packaging and test method.
Our team will perform a leak test and provide a recorded test video, allowing you to assess performance and application fit before making a decision.