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Modernization of Cosmetics Regulation Act

This whitepaper outlines the shift in cosmetics oversight by the U.S. FDA.

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Whitepaper //

Modernization of Cosmetics Regulation Act

This whitepaper outlines the shift in cosmetics oversight by the U.S. FDA.

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Whitepaper //

The EU Clinical Trials Regulation

This paper provides changes and updates to Clinical Trials Regulation in the EU as of December 2023.

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Safety Assessment of E-Cigarettes in the EU

This whitepaper outlines safety requirements and key considerations in exposure assessments, hazard identification and risk assessments for e-cigarettes…

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Safety Assessment of E-Cigarettes in the US

This whitepaper outlines safety and risk assessments as well as literature monitoring for e-cigarettes in the US.

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Preparing FDA Submission Data Packages

This paper describes the evolution of data standards and recommends best practices in planning and preparing FDA submission…

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ClinChoice PV Facing Pandemic Whitepaper

This whitepaper describes the role of pharmacovigilance in our modern world and the need for evolution in drug…

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Tailored Functional Service Whitepaper

This whitepaper examines the characteristics of various FSP models and how they help bring new therapies to market…

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Review of QA on regulations for Custom …

This review explores questions and considerations around custom-made, adaptable, and patient-matched medical devices.

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