The understanding and evaluation of the regulatory environment for every new product is a complex and intimidating process. Our consulting teams can play a key role on your projects and provide you with support during both clinical development and regulatory approvals.
A wealth of information
Our consulting teams have a wealth of information in all disciplines and therapeutic areas enabling them to direct well-designed clinical development programs, and interpret results in a timely and efficient manner. Our team has the experience, technical ability, passion and commitment you expect from your own employees.
Advice on overcoming hurdles
Many obstacles can delay research and development or prevent products from reaching their full market potential. These hurdles might be related to drug safety, dose regimen, clinical planning or fundamental strategic approaches. Accovion can advise you on how to overcome these obstacles.
The right solutions
Finding the right solutions is our business. When it comes to regulatory matters, you can benefit from Accovion’s years of experience and outstanding expertise. We are proud of our distinguished reputation for Regulatory Consulting services and are ready to assist you in creating and following a strategy for success.
Accovion’s team of scientific, regulatory, clinical and biostatical professionals possess the experience, insight and knowledge necessary to help you reach strategic milestones.
Dr. Rainer Porrmann
Manager Study Coordination & Clinical Trial Submission
+49 6196 7709-385
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