PROMETRIKA, LLC is a distinguished full-service clinical research organization (CRO) headquartered in Cambridge, Massachusetts. With a robust focus on the pharmaceutical and biotechnology industries, PROMETRIKA offers a comprehensive suite of services designed to support the entire clinical trial process. Their expertise spans clinical operations, pharmacovigilance, data management, biostatistics, medical writing, and regulatory submissions, making them a versatile partner for companies navigating the complexities of drug development.
At PROMETRIKA, the commitment to excellence is evident in their meticulous approach to managing clinical trials. They leverage advanced technologies and methodologies to ensure the integrity and accuracy of medical data, which is critical for successful regulatory submissions. Their team of seasoned professionals excels in analyzing and interpreting clinical data, providing valuable insights that drive informed decision-making for their clients.
In addition to their core services, PROMETRIKA is dedicated to fostering strong partnerships with client companies and institutions, enabling them to meet their research goals efficiently and effectively. By utilizing innovative data management systems and biostatistical techniques, they enhance the quality of clinical research while ensuring compliance with industry regulations. PROMETRIKA's dedication to advancing healthcare through rigorous clinical research positions them as a trusted ally in the quest for new therapies and treatments, ultimately contributing to improved patient outcomes. For more information, visit their website at http://www.PROMETRIKA.com.
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51-200 employees
View all PROMETRIKA, LLC employees
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Biotechnology
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100 CambridgePark Drive, Second Floor, Cambridge, MA 02140, US
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2003
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Medical Writing, Biostatistics, Clinical Monitoring, Clinical Operations, Clinical Data Management, Regulatory Submissions, Statistical Programming, Regulatory Submissions, Database Programming, Medical Writing, Database Programming, Data Monitoring Committee (Dmc), Electronic Data Capture (Edc), Nda & Eu Regulatory Submissions, Clinical Monitoring, Electronic Data Capture (Edc), Clinical Data Management, Statistical Programming, Biostatistics, Cdisc Stdm & Adam, Clinical Operations
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Miganush Stepanians is the CEO of PROMETRIKA, LLC. To contact Miganush Stepanians email at [email protected].
The decision makers in PROMETRIKA, LLC are Barry Mirrer, Cathy Hult, Chris Gallant, etc. Click to Find PROMETRIKA, LLC decision makers emails.
You can reach PROMETRIKA by visiting their website at www.PROMETRIKA.com and using the contact form provided. Alternatively, you can call their main office or send an email to their designated contact address for prompt assistance regarding their services.
Yes, PROMETRIKA provides a staff directory on their website, showcasing the expertise and roles of their team members. This resource helps clients understand who to contact for specific inquiries related to clinical operations, biostatistics, medical writing, and more.
PROMETRIKA primarily serves the pharmaceutical and biotechnology industries. Their comprehensive services support clients in clinical trials, regulatory submissions, and data management, ensuring compliance and efficiency throughout the research process.
PROMETRIKA offers a full range of services for clinical trials, including clinical operations, pharmacovigilance, data management, biostatistics, medical writing, and regulatory submissions. Their expertise ensures that trials are conducted efficiently and in compliance with industry standards.
To find specific team members at PROMETRIKA, you can visit their staff directory on the website. This directory lists employees along with their roles and areas of expertise, making it easier to identify the right contact for your needs.
For inquiries about regulatory submission services, you can fill out the contact form on PROMETRIKA's website or directly email their regulatory affairs team. They will provide detailed information and guidance tailored to your specific submission requirements.
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