Tamper-proof Pharmaceutical Packaging

There is hardly another product that reaches consumers or patients for which packaging requirements are as varied as for pharmaceutical products. The »Poisons Prevention Packaging Act« (PPPA) enacted in the United States back in 1970 addresses the issue of child-resistant packaging of substances that are potentially harmful to human health.

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ViroPharma Incorporated

Shire acquired ViroPharma on February 20, 2015. Following this date, this page will no longer be actively monitored. There will be no updates or responses posted on this page.

OTHER WHITEPAPERS
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Overcoming technical challenges in cell-based high throughput screens

whitePaper | November 11, 2022

Tremendous technological advancements in automated biotechnology and combinatorial chemistry have led to the widespread implementation of high throughput screening (HTS) for drug discovery since the early 1990s.

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Seize the digital momentum

whitePaper | January 23, 2023

Investments in biopharmaceutical (biopharma) research and development (R&D) continue to fuel innovation and shape the future of health. However, this year’s analysis demonstrates that despite impressive examples of innovative products the step-change in improved productivity seen in 2021 has not continued.

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Protein fingerprints pave the way for microarray comparison

whitePaper | June 9, 2022

Anaxomics has developed a novel method of analysis for microarray data based on the generation and subsequent comparison of 2D fingerprints for each sample. Microarray results are incorporated into a protein interaction network and embedded with all sorts of biological and medical data.

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Characterization of Protein Aggregates and Other Particles in Biopharmaceuticals

whitePaper | July 8, 2022

Particulates are ubiquitous in parenteral drug products and remain a concern throughout their development and production1–3. These particles must be monitored to satisfy.

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Advancing drug development using in silico modeling

whitePaper | June 22, 2022

The technologic and pharmacologic advances that have enabled researchers to take aim at previously untreatable diseases have contributed to an increase in the number of molecules in the development pipeline that are challenging and difficult to manufacture.

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Asia Pacific as a Clinical Trials Powerhouse

whitePaper | October 6, 2022

Patient availability is a critical component for clinical trials, and so it stands to reason that clinical development should match the epidemiology of diseases. Of course, this is often not the case,

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Spotlight

ViroPharma Incorporated

Shire acquired ViroPharma on February 20, 2015. Following this date, this page will no longer be actively monitored. There will be no updates or responses posted on this page.

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