ClinDatrix, Inc. is a privately held, full-service CRO founded in 2002 to help drug and medical device innovators advance their therapeutic products toward regulatory approval.
|Industry||Project Management, Clinical Monitoring, Medical Monitoring and Patient Safety, Data Management, Biostatistics, Medical Writing, Regulatory Affairs, Quality Assurance, Preclinical Development Consulting, and Investigator Meeting Planning|
|Number of employees||11-50 employees|
ClinDatrix, Inc. helps drug and medical device innovators advance their therapeutic products toward regulatory approval.
Over the past decade, ClinDatrix has grown to offer contract research expertise from preclinical development guidance through regulatory filings and post-marketing studies. They continue to work primarily with small to mid-sized companies, a subset of innovators we know and serve very well. We also are a reliable resource to large pharma and medical device companies seeking to outsource specialized tasks for timely completion.
ClinDatrix is committed to providing world class, full service clinical research capabilities to the biotechnology, medical device and pharmaceutical industries.
Partnering they use a personalized approach while in partner with their clients to apply knowledge and experience to the goals of managing, monitoring, collecting, validating, analyzing, reporting and delivering quality clinical data with efficiency and accuracy.
The company has always been known for their quality, integrity, flexibility, knowledge and experience, ClinDatrix is a trusted service provider in clinical research, medical safety, data management, statistical analyses, regulatory affairs and quality assurance. ClinDatrix has established a strong reputation as a CRO made up of committed professionals who understand the technical requirements, business considerations and regulatory parameters of the pharmaceutical, biotechnology and medical device industries. Moreover, they combine teamwork and efficiency with a single-minded focus on customer satisfaction to address each of our client's specific needs.
ClinDatrix hires and engages clinical, medical safety, data, statistical and regulatory personnel who are technically and clinically knowledgeable and who have relevant, hands-on experience in clinical product development. As a result, the ClinDatrix team offers broad experience from across the biotechnology, pharmaceutical and medical device industries.
Our skilled and talented team members are among the finest of CRO practitioners. They use best practices to achieve successful results for clinical investigations of all levels of size, complexity and scope. Beyond being leaders in their respective disciplines, our personnel are trained in ClinDatrix systems and processes and cross-trained in other functions to enhance their overall knowledge and experience of the clinical development process.
- project management
- event planning
- clinical monitoring
- medical safety
- data management
- medical writing
- regulatory affairs
- quality assurance
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