About Us

Our Company Mission

Our Mission is to help our clients bring promising products into the market as quickly as possible ensuring regulatory compliance.  Our passion is not only helping you throughout your drug development journey but also to keep the patients in mind and making sure the product is safe and effective.

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ClinReg Partners Consulting is committed to the success of your products and provide experts in developing and implementing required regulatory and quality solutions for your needs. Our team bring several years of combined experience in Regulatory Affairs, Quality Assurance, and Clinical Research with a proven track record of executing global strategy techniques in a timely and cost-efficient manner.  

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Our subject matter experts have years of experience working with many small to large companies, advising on the US FDA, and EU Competent Authorities Marketing authorization process. 

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With our experience, regardless of where you are in the process of your drug development, we are well-equipped to provide clinical regulatory advice for successful regulatory submissions, such as IND, CTA, NDA, and BLA applications.

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Our team of experts has experience in many different therapeutic areas such as oncology, cardiovascular, dermatology, gastroenterology, orthopedic, ophthalmology, CNS, and more.  

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ClinReg Partners can handle multiple aspects of your drug development from discovery to post-marketing surveillance activities.