Berry Consultants is a statistical consulting company specializing in innovative clinical trial design, analysis, execution, and software solutions for the pharmaceutical and medical device industry. Berry Consultants’ primary services include designing adaptive clinical trials, conducting comparative effectiveness research such as decision analysis and meta-analysis, providing strategic operational excellence and knowledge of advanced trial implementation, supporting interim analysis and trial updates during the execution of adaptive trials, participating on Data Monitoring Committees, and licensing FACTS (Fixed and Adaptive Clinical Trial Simulator) software which is the most powerful, flexible, and fastest simulation tool on the market for advanced clinical trial design. The Berry Consultants team has extensive experience in working with clinical investigators, scientific domain experts, FDA, and EMA in the design, simulation, and implementation of complex adaptive clinical trials that range from proof of concept studies to some of the most innovative multi-drug platform trials.
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11-50 employees
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Pharmaceutical Manufacturing
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3345 Bee Caves Road, Suite 201, Austin, Texas 78746, US
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2000
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Simulation Software, Clinical Trial Simulation, Medical Statistics, Adaptive Clinical Trial Design, Bayesian Approach
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The decision makers in Berry Consultants, LLC are Doray Sitko, Melanie Quintana, Michelle Detry, etc. Click to Find Berry Consultants, LLC decision makers emails.
Berry Consultants specializes in innovative clinical trial designs, including adaptive clinical trial designs and Bayesian approaches. These methodologies allow for more flexible and efficient trials, enabling adjustments based on interim results to optimize outcomes and resource utilization.
Berry Consultants employs advanced simulation software to model various clinical trial scenarios. This allows clients to assess the potential outcomes of different designs, identify optimal strategies, and make informed decisions before actual trial execution. Simulation helps in understanding the implications of design choices on trial success and regulatory approval.
Berry Consultants primarily serves the pharmaceutical and medical device industries. Their expertise in statistical consulting and clinical trial design is tailored to meet the unique challenges and regulatory requirements of these sectors, ensuring that clients can effectively bring their products to market.
Yes, Berry Consultants provides support for regulatory submissions by ensuring that clinical trial designs and analyses meet the necessary standards set by regulatory bodies. Their expertise in medical statistics and adaptive trial designs helps clients prepare comprehensive documentation that enhances the likelihood of successful approvals.
The Bayesian approach is a statistical method that incorporates prior knowledge and evidence into the analysis of clinical trial data. Berry Consultants utilizes this approach to provide more robust and flexible analyses, allowing for real-time updates and adjustments to trial designs based on accumulating data. This can lead to more informed decision-making and potentially faster pathways to market.
To get started with Berry Consultants, you can visit their website and fill out the contact form or reach out directly via email or phone. A team member will connect with you to discuss your specific needs, project goals, and how Berry Consultants can provide tailored solutions to support your clinical trial initiatives.
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