USDM provides GCP services tailored to the needs, size, and resources of your company.
The USDM team uses a proactive approach to compliance and quality assurance that ensures efficient processes for your drug development and submission activities. We identify compliance issues that are relevant to your organization, assess compliance issues and their relationship to other potential concerns, develop a strategic compliance management plan for your company, and ensure continuous compliance.
Regulatory approval processes are complex to navigate, often resulting in costly delays. USDM’s GCP experts can help you gain a solid understanding of global regulations to ensure that your clinical activities are in compliance. Having worked with companies of all sizes in all regulated fields (including clinical trials, medical devices, and biological products), USDM is equipped to assist in every aspect of internal GCP auditing, analysis, corrective actions, process development, and training.
to see how we can address your GCP needs.