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.See Our Expanded Services
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.
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.