seo-company

Medicor Research Inc.

Medicor Research Inc. provides a system where pharmaceutical sponsors work directly with physicians but also have the systematic, organized and dedicated system of a Site Management Organization (SMO...load more

Medicor Research Inc.'s Basic Information

Industry
Pharmaceutical Manufacturing
Headquarters
Ontario, Canada
Website
http://medicorresearch.com
Linkedin
https://www.linkedin.com/company/medicor-research-inc./
Founded Year
2005
Headcount
11 - 50 ( View All )
Specialties
Coordination of Phase II, III and IV Clinical Trials.Data management of clinical trials.A 12 hr/day safety monitoring system is available for study subjects with a qualified physician on-site 7 days a week.Patient access to an on-call nurse 24 hrs/day.

Medicor Research Inc.'s Competitors

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Eepi GmbH
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Trident Clinical Research
Trident Clinical Research

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Chesil Consultants
Chesil Consultants

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Employee Insights

Employee Function
Employee Location
View Employee Insights

Medicor Research Inc.'s Top Employees

people

Shelley Chenard

Director OF Clinical Development

Phone Email

people

Shelley Chenard

Director OF Clinical Development AND Recruitment

Phone Email

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Frequently Asked Questions Regarding Medicor Research Inc.

Where is Medicor Research Inc.'s headquarter located?
Medicor Research Inc.'s headquarter are located at Canada.
How many employees does Medicor Research Inc. have?
Medicor Research Inc. has 11 - 50 employees.
What is Medicor Research Inc.'s official website?
Medicor Research Inc.'s official website is http://medicorresearch.com
What industry does Medicor Research Inc. belong to?
Medicor Research Inc. is in the industry ofPharmaceutical Manufacturing
What does Medicor Research Inc. do?
Medicor Research Inc. provides a system where pharmaceutical sponsors work directly with physicians but also have the systematic, organized and dedicated system of a Site Management Organization (SMO...
What specialty does Medicor Research Inc. have?
Coordination of Phase II, III and IV Clinical Trials.Data management of clinical trials.A 12 hr/day safety monitoring system is available for study subjects with a qualified physician on-site 7 days a week.Patient access to an on-call nurse 24 hrs/day.
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