Clinvax Clinical Trials Solutions

Clinvax Clinical Trials Solutions

Research, 1708 Spring Green BLVD, Katy, Texas, 77494, United States, 51-200 Employees

clinvax.com

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phone no Phone Number: +19*********

Who is CLINVAX CLINICAL TRIALS SOLUTIONS

ClinVax is a Site Network that specializes in Clinical Trial management on all Phases(I-IV) of drug development. Our main focus is to be a go-to resource for sites, pharmaceutical, biotec...

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  • 1708 Spring Green BLVD, Katy, Texas, 77494, United States Headquarters: 1708 Spring Green BLVD, Katy, Texas, 77494, United States
  • 2017 Date Founded: 2017
  • 51-200 Employees: 51-200
  • dollar-icon Revenue: $250 Million to $500 Million
  • tech-icon Active Tech Stack: See technologies

industries-icon Industry: Research

SIC SIC Code: 8711 | NAICS Code: 541330 | Show More

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Employees

Sharon Dawson

Director of Clinical Trials

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Frequently Asked Questions Regarding Clinvax Clinical Trials Solutions

Answer: Clinvax Clinical Trials Solutions's headquarters are located at 1708 Spring Green BLVD, Katy, Texas, 77494, United States

Answer: Clinvax Clinical Trials Solutions's phone number is +19*********

Answer: Clinvax Clinical Trials Solutions's official website is https://clinvax.com

Answer: Clinvax Clinical Trials Solutions's revenue is $250 Million to $500 Million

Answer: Clinvax Clinical Trials Solutions's SIC: 8711

Answer: Clinvax Clinical Trials Solutions's NAICS: 541330

Answer: Clinvax Clinical Trials Solutions has 51-200 employees

Answer: Clinvax Clinical Trials Solutions is in Research

Answer: Clinvax Clinical Trials Solutions contact info: Phone number: +19********* Website: https://clinvax.com

Answer: ClinVax is a Site Network that specializes in Clinical Trial management on all Phases(I-IV) of drug development. Our main focus is to be a go-to resource for sites, pharmaceutical, biotechnology, and medical device companies in ensuring a successful outcome of Clinical Trials. Our Site Network management is distinct as we are committed to providing experts that assists with site initiation, database combing, patient identification, recruitment and enrollment, study patient facing material drafting, EDC study compliance review, protocol writing and review, data collection, management and analyses. This way clinical trials flow smoothly with minimal deviations with eventual reduction in bench-to- bedside time for Investigational Products. We are a highly experienced network of sites that have been involved in various clinical studies in different therapeutic areas and indications. Our certified medical experts are committed to providing the highest quality of service by ensuring safety of patients, validity of data and conduct of clinical trials per protocol and in accordance to the ICH- GCP guidelines. It gives us great gratification to be part of a solution.

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