Southwood Research has joined ProPharma Group Regulatory Sciences

Since 2016, Southwood Research has focused on understanding the science behind every product and providing clients like you with strategic clinical and regulatory insights. These expert EMA/EU regulatory affairs partners have joined ProPharma Group, together forming the world’s leading provider of regulatory services for clients seeking consulting expertise with the Food and Drug Administration (FDA), European Medicines Agency (EMA), and national agencies throughout Europe. You’ll find the same experienced, scientific approach from our experts, along with elevated services to support your regulatory needs anywhere in the world. See Our Expanded Services

Supporting successful outcomes

We develop product development and regulatory strategies based on a solid scientific foundation, helping to ensure regulatory and market success from pre-approval of your product or medical device through post-approval launch, line extensions, and maintaining optimal regulatory status for both the FDA and EMA.

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Your single-source service provider

ProPharma Group is the global, independent provider of regulatory sciences, clinical research solutions, life science consulting, pharmacovigilance, and medical information services serving pharmaceutical, biotechnology, and medical device companies.

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Need Help Navigating the Dynamic Regulatory Market to Bring Your Product Concept to Market?

Contact us today to discover how 35+ years of regulatory experience using a strategic and scientific approach can deliver successful and expeditious outcomes.

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