TPS's Advanced EVOH Solutions for Pharmaceutical Primary Packaging

The company's pharmaceutical-grade Evoh Resins are manufactured under cGMP conditions and undergo extensive validation to ensure compliance with:

- European Pharmacopoeia requirements

- USP standards

- FDA regulations for drug packaging

- ICH guidelines for stability testing

TPS implements a comprehensive quality management system that includes:

- Detailed material characterization

- Stability testing protocols

- Full traceability documentation

- Validated cleaning procedures

- Environmental monitoring systems

One of TPS's major achievements in pharmaceutical packaging is the development of moisture-resistant EVOH grades specifically designed for hygroscopic drug protection. These innovative materials maintain their barrier properties even under challenging environmental conditions, with relative humidity levels up to 85%. Independent studies have demonstrated superior protection compared to conventional barrier materials, with moisture vapor transmission rates below 0.2 g/m²/day.

The company's pharmaceutical portfolio includes specialized grades for blister packaging applications, featuring:

- Enhanced thermoforming characteristics

- Superior cavity definition

- Excellent delamination resistance

- Consistent barrier properties post-forming

TPS's technical service team provides comprehensive support for pharmaceutical packaging development, including:

- Material selection guidance

- Process optimization recommendations

- Stability testing protocols

- Regulatory compliance support

- Validation assistance

Recent innovations from TPS include the development of EVOH grades with enhanced chemical resistance for aggressive drug formulations. These materials demonstrate excellent compatibility with:

- Active pharmaceutical ingredients

- Common excipients

- Preservatives

- Stabilizers

The company's research has shown that these chemical-resistant grades maintain their structural integrity and barrier properties even after prolonged contact with challenging drug formulations. This performance is crucial for ensuring product stability throughout the intended shelf life.

TPS's commitment to pharmaceutical packaging excellence extends to their development of clean processing grades that minimize particulate generation during manufacturing. These materials feature:

- Reduced gel content

- Improved filtration characteristics

- Enhanced thermal stability

- Consistent processing behavior

The company's technical experts work closely with pharmaceutical manufacturers to optimize processing conditions and ensure consistent quality in high-speed production environments. This collaboration has resulted in successful implementations across various pharmaceutical packaging applications.