Clinical Monitoring Change Management

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Translating regulatory guidance into success for your organization is difficult when there is not a consistent industry standard. Coupled with new processes and procedures within a company that has a risk-averse culture, success seems nearly impossible. However, that is not the case when working with ProPharma's team of clinical research experts.

Regardless of the specifics your organization is facing, we have the experience to help you overcome your current challenges. Learn how ProPharma can work with you to design and implement successful operating models, and develop consistent global processes, procedures, and validated tools to ensure your organization is aligned with regulatory requirements and industry standards.

Case Study


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The Cost of Poor Project Management

Project Management isn’t for the faint of heart. There is a shockingly high rate of project failure… but on the other hand, great project management can be a key differentiator that leads a company...

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Successfully Passing MHRA Inspections for Overseas Manufacturing Sites

ProPharma offers GMP and GDP compliance services from clinical development to commercial distribution of the products' lifecycle. ProPharma’s Compliance and Quality team completed the first on-site...

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Navigating the Generic Drug Application and Approval Process

Navigating the generic drug application and approval process can be challenging. From pre-filing through post-approval, find out exactly what needs to be done for your Abbreviated New Drug...