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Untangling the Complexities of Cell and Gene Therapy Clinical Trials: A Supply Chain Perspective 

Pharmaceutical Technology

By Luisa Sterkel & Joana Loureiro , Tenthpin Consultants The promise and potential of cell and gene therapies (CGT) has emerged in the recent past and currently over 1.500 CGT are registered for clinical trials holding great hope for the treatment of challenging and uncurable diseases. plan a, plan b, … charter flight standby option).

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Clinical Trial Data: Navigating Audit Trail Data Regulations and Accessibility Challenges 

VirTrial

Study data is always subject to scrutiny by regulators, which further highlights its importance. Given the industry is a highly regulated one, there are always new regulations being issued. Given these regulations are not new, it is strange that industry has not prompted a complete solution to this already.

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Why and How Will Ecommerce Transform the Interactive Response Technology (IRT) User Experience?

XTalks

IRT solutions help clinical trial sponsors meet the complexities of patient randomization and clinical supply management. He also shared how modern software development concepts are impacting IRT platforms and transforming the user experience in clinical trials. This ultimately helps to get medicines to the market faster.

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Clinical Trial Data: Navigating Audit Trail Data Regulations and Accessibility Challenges 

VirTrial

Study data is always subject to scrutiny by regulators, which further highlights its importance. Given the industry is a highly regulated one, there are always new regulations being issued. Given these regulations are not new, it is strange that industry has not prompted a complete solution to this already.

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Clinical Trial Data: Navigating Audit Trail Data Regulations and Accessibility Challenges 

VirTrial

Study data is always subject to scrutiny by regulators, which further highlights its importance. Given the industry is a highly regulated one, there are always new regulations being issued. Given these regulations are not new, it is strange that industry has not prompted a complete solution to this already.

article thumbnail

Clinical Trial Data: Navigating Audit Trail Data Regulations and Accessibility Challenges 

VirTrial

Study data is always subject to scrutiny by regulators, which further highlights its importance. Given the industry is a highly regulated one, there are always new regulations being issued. Given these regulations are not new, it is strange that industry has not prompted a complete solution to this already.

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Africa: Unleashing the potential of the new superpower in clinical trials

Pharmaceutical Technology

Africa has considerable advantages and opportunities for trialling investigational medicinal products that, if pharma companies can correctly harness, will turn the continent into a superpower for clinical trials. They need to have that assistance of access to clinical trials.”