White Papers

  1. Blow-Fill-Seal For Biologics: Breaking Through In Pharma Packaging
    5/3/2017

    As the industry continues its move toward biologics, innovative solutions and technologies will be needed to ensure a safe and reliable approach to the manufacturing and delivery of these drugs. 

  2. The Impact Of Patient Compliance On Pharma Manufacturers
    5/2/2017

    In fact, patient non-compliance is the fourth leading cause of death in the United States, and the annual cost of non-compliance in the U.S. is estimated to be $317 billion and $125 billion in the EU.

  3. Manufacturing Plants Based On The Lego Principle
    5/2/2017

    Small batches and multiple products in the same plant — these are the market demands to which more and more manufacturers need to adjust. The answer is based on the "Lego principle."

  4. Designing For Moldability: Volume 1 - A Rapid Injection Molding Reference Guide For Product Designers And Engineers
    5/1/2017

    This quick-reference user guide, for engineers and designers, talks about the guidelines and limitations for rapid injection molding. Learn how to get the best possible results for your real plastic molded parts.

  5. Planning And Executing Cycle Development For The Vapor Hydrogen Peroxide Decontamination Of A Filling Line Isolator
    4/6/2017

    The cycle development approach described in this document is fairly universal and should not be dependant on individual isolator systems. The terminology used may be slightly different depending on the technology.

  6. How To Reduce Costly Scale-Up Problems in Solid Dose Manufacturing
    4/4/2017

    Problems with capping/lamination and sticking/ picking are often first realized when a formulation is introduced to a level of compression required to supply market demand.

  7. Validation, Verification, And Monitoring For Product Inspection Equipment
    3/16/2017

    This white paper gives guidance on the essential processes of validation, verification, and routine performance monitoring for in-line product inspection equipment in food making facilities.

  8. Broaden Analysis Of Compound Factors For Predictive Solubility Solutions
    3/2/2017

    Developed by the FDA, the Biopharmaceutics Classification System helps companies when they file for bioequivalence of dosage forms based on in vitro dissolution testing.

  9. Security Of Pharmaceuticals: A Comparison Of EU And US Standards
    2/27/2017

    Europe and the United States are considered the world leaders in the safest pharmaceutical markets for patients. However, the US and Europe are also a lucrative target for drug crime.

  10. Optimize Your Critical Cleaning Process And Ensure Results
    2/2/2017

    Getting the best results from any cleaner requires proper mixing and cleaning procedures. This article includes mixing directions for aqueous cleaning detergent and methods for monitoring performance.