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The Weinberg Group has joined ProPharma Group Regulatory Affairs

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

Our compliance consultants 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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