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Southwood Research has joined ProPharma Group Regulatory Affairs

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.

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Supporting successful outcomes

We develop regulatory strategies based on a solid scientific foundation, helping to ensure regulatory 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.

View Our Full Suite of Regulatory Affairs Services

Your single-source service provider

ProPharma Group provides regulatory, compliance, pharmacovigilance, and medical information services to help improve patient health and safety at every step throughout the product lifecycle.

See How We Help At Every Step

Your Business has Complex Challenges. ProPharma Group has Exceptional Solutions.

We partner with pharmaceutical, biotechnology, and medical device clients to tackle complex challenges. Contact us to learn how our experienced team can help ensure regulatory and development success throughout the product lifecycle.

Interested in gaining an industry edge? Let us help you stay up to date.


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