Selection Criteria for Use of Third-Party Laboratories
The recently issued and very uncommon Food and Drug Administration
USP <661.2> Testing of Blister Cards
When the proposed final drafts of USP <661.1> and <661.2>
Vial Dimensions and their Impacts on Container Closure Integrity
Package Development and Validation Studies USP <1207> discusses best practices
Package Distribution Testing – Recent Changes to ASTM D4169 Testing Requirements
Package (shipment) Distribution Testing is designed to simulate the distribution environment
CS Analytical – How We Are Different
Even as CS Analytical is truly unique as the world’s
Extensive Knowledge & Experience with a Wide Variety of Drug Product Package System
The CS Analytical is the only FDA Regulated, cGMP contract
Meet members of our All-Star team of package professionals
The CS Analytical is the only FDA Regulated, cGMP
Dose Accuracy Testing
Understanding Deliverable Volume and Uniformity of Dosage Deliverable volume
Critical Considerations in Choosing a USP <1207> Container Closure Integrity Testing Laboratory
Written By BRIAN MULHALL / Chief Executive Officer As outlined