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The Weinberg Group has joined ProPharma Group Regulatory Sciences

For over 35 years, The Weinberg Group’s FDA consultants have ensured clients like you achieve their drug and device development goals. The Weinberg Group’s expert regulatory consultants have now joined ProPharma Group; together forming the world’s leading provider of regulatory services for clients seeking compliance consulting with the FDA, EMA, and national agencies throughout Europe.

Our experienced team of FDA and EMA consultants can work with you to develop regulatory strategies; prepare submissions; and remediate, maintain, and improve regulatory compliance.

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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?

Complete the form or call us at 202-833-8077 to discover how 35+ years of regulatory experience using a strategic and scientific approach can deliver successful and expeditious outcomes.

Interested in gaining an industry edge? Let us help you stay current.


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