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Research ArticleTECHNOLOGY/APPLICATIONS

Automated Method for Determining Instron Residual Seal Force of Glass Vial/Rubber Closure Systems Part II. 13 mm vials

John D. Ludwig and Craig W. Davis
PDA Journal of Pharmaceutical Science and Technology September 1995, 49 (5) 253-256;
John D. Ludwig
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Craig W. Davis
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Article Information

vol. 49 no. 5 253-256
PubMed 
7489201

Published By 
Parenteral Drug Association (PDA)
Print ISSN 
1079-7440
Online ISSN 
1948-2124
History 
  • Received January 30, 1995
  • Accepted March 27, 1995
  • Published online September 1, 1995.

Copyright & Usage 
Copyright © Parenteral Drug Association. All rights reserved.

Author Information

  1. John D. LudwigΔ and
  2. Craig W. Davis
    1. Δ Author to whom correspondence should be addressed: Searle, 4901 Searle Parkway, Skokie, IL 60077.

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    PDA Journal of Pharmaceutical Science and Technology
    Vol. 49, Issue 5
    September-October 1995
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    Automated Method for Determining Instron Residual Seal Force of Glass Vial/Rubber Closure Systems Part II. 13 mm vials
    John D. Ludwig, Craig W. Davis
    PDA Journal of Pharmaceutical Science and Technology Sep 1995, 49 (5) 253-256;
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    Cited By...

    • Container Closure Integrity of Vial Primary Packaging Systems under Frozen Storage Conditions: A Case Study
    • Quantifying the Vial-Capping Process: Reexamination Using Micro-Computed Tomography
    • Balancing Container Closure Integrity and Aesthetics for a Robust Aseptic or Sterile Vial Packaging System
    • Residual Seal Force Testing: A Suitable Method for Seal Quality Determination of (High Potent) Parenterals
    • The Pharmaceutical Capping Process--Correlation between Residual Seal Force, Torque Moment, and Flip-off Removal Force
    • Influence of Different Container Closure Systems and Capping Process Parameters on Product Quality and Container Closure Integrity (CCI) in GMP Drug Product Manufacturing
    • Impact of Vial Capping on Residual Seal Force and Container Closure Integrity
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    More in this TOC Section

    • Evaluation of Steam Sterilization Processes: Comparing Calculations Using Temperature Data and Biointegrator Reduction Data and Calculation of Theoretical Temperature Difference
    • Optimization of the Drug Solution Preparation Process for a Production-Scale Crossflow Ultrafiltration System
    • Bacterial Adhesion: Considerations Within A Risk-Based Approach To Cleaning Validation
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    Automated Method for Determining Instron Residual Seal Force of Glass Vial/Rubber Closure Systems Part II. 13 mm vials
    John D. Ludwig, Craig W. Davis
    PDA Journal of Pharmaceutical Science and Technology Sep 1995, 49 (5) 253-256;

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