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ethica CRO

ethica CRO is a full-service Contract Research Organization (CRO) that conducts and manages ethical clinical research on behalf of sponsors within the international pharmaceutical, biotechnology, medical device, nutraceutical, and cosmeceutical industries

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CONTACTS AT ETHICACRO.COM

Ethica Clinical Research inc

Janice Parente

8555 Tr●●●●●●●ada Hwy

Sui●●●201

Mon●●●eal , Quebec, H4S 1Z6

Canada

1.51●●●●0442
jp●●●●●●@ethicaclinical.ca

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Ethica Clinical Research inc

Janice Parente

8555 Tr●●●●●●●ada Hwy

Sui●●●201

Mon●●●eal , Quebec, H4S 1Z6

Canada

1.51●●●●0442
jp●●●●●●@ethicaclinical.ca

View this contact

Ethica Clinical Research inc

Janice Parente

8555 Tr●●●●●●●ada Hwy

Sui●●●201

Mon●●●eal , Quebec, H4S 1Z6

Canada

1.51●●●●0442
jp●●●●●●@ethicaclinical.ca

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ethica CRO | ethicacro.com Reviews
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ethica CRO is a full-service Contract Research Organization (CRO) that conducts and manages ethical clinical research on behalf of sponsors within the international pharmaceutical, biotechnology, medical device, nutraceutical, and cosmeceutical industries
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1 ethica
2 CRO
3 contract research organization
4 clinical study management
5 biometrics
6 feasibility assessment
7 protocol development
8 study start-up
9 project management
10 study monitoring
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ethica cro,research participants,press room,careers,the ethica cro,difference,management,research experience,accreditation,clinical study,feasibility assesment,protocol development,study start up,project management,study monitoring,regulatory affairs
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ethica CRO | ethicacro.com Reviews

https://ethicacro.com

ethica CRO is a full-service Contract Research Organization (CRO) that conducts and manages ethical clinical research on behalf of sponsors within the international pharmaceutical, biotechnology, medical device, nutraceutical, and cosmeceutical industries

INTERNAL PAGES

ethicacro.com ethicacro.com
1

Project Management

http://ethicacro.com/clinical-study/project-management.php

Our experienced and highly-qualified project managers ensure that your study timelines are met. Study-specific tools are created to track and manage study metrics such as, enrolment status, essential documents, monitoring, participant and CRF tracking, drug accountability, data queries, and adverse events. The ethica CRO Difference. Ethica Clinical Research Inc.

2

Study Monitoring

http://ethicacro.com/clinical-study/study-monitoring.php

Our full-service clinical monitoring is conducted in accordance with a well-designed monitoring plan, ICH-GCP Guidelines, applicable regulatory requirements, and our accredited SOPs. Our on-site study monitoring services include:. Qualification visits (see Study Start-up). The ethica CRO Difference. Ethica Clinical Research Inc.

3

ethica CRO

http://ethicacro.com//fr

Participants à la recherche. Évaluation de faisabilité. Ethica CRO est un organisme de recherche sous contrat (ORC) à service complet qui effectue et gère des recherches cliniques éthiques au nom de promoteurs dans les industries suivantes : pharmaceutique, biotechnologique, dispositifs médicaux, nutriceutique et cosmétique. Le bien-être des participants à la recherche est d'une importance primordiale. Une équipe de gestion ayant une expertise scientifique exhaustive. Ethica CRO est un organisme de reche...

4

Regulatory Affairs

http://ethicacro.com/clinical-study/regulatory-affairs.php

Our regulatory affairs staff provides expert consulting and assistance to ensure that you are in compliance with the requirements of regulatory agencies worldwide, including:. Clinical Trial Submissions (CTA, IND). Labeling of clinical trial materials. Regulations and guidelines governing clinical trials. Maintenance and archiving of documents. The ethica CRO Difference. Ethica Clinical Research Inc.

5

Data Management

http://ethicacro.com/biometrics/data-management.php

Ethica CRO's experienced data management team will guide you in selecting the best data collection tools for your budget and timelines. Our computerized systems meet the industry's highest standards and are all 21 CFR Part 11 compliant. As a result of an ongoing training program, the members of our data management team are experts in the use of commercial clinical data management systems such as Oracle Clinical as well as our proprietary in-house systems. Data management and validation plan development.

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LINKS TO THIS WEBSITE

veritasirb.com veritasirb.com

Veritas - IRB Roster

http://www.veritasirb.com/ethics-review/irb-roster.php

The Veritas IRB Difference. The IRB is a multidisciplinary group comprised of men and women with extensive knowledge of clinical research, medicine, dentistry, pharmacology, biomedical sciences, genomics, alternative medicine/natural health, ethics, law, and social sciences. Veritas IRB board members are not employees of Veritas IRB Inc. The Veritas IRB Difference. Ethica Clinical Research Inc.

veritasirb.com veritasirb.com

Institutional Services

http://www.veritasirb.com/institutional-services/index.php

The Veritas IRB Difference. For many hospitals, operating an efficient ethics review unit is a complex and challenging task. This challenge can even be greater when the volume of research does not allow for regular meetings or maintenance of full-time personnel. Veritas IRB's Institutional Services include the following:. Meeting with your Institution's officials. Auditing your Institution's IRB's records. Developing institution-specific Standard Operating Procedures (SOPs). The Veritas IRB Difference.

veritasirb.com veritasirb.com

Ethics Review Services in the United States

http://www.veritasirb.com/international-services/united-states.php

The Veritas IRB Difference. In the United States. With Veritas IRB's North American panel composed of US board-certified physicians, we can provide thorough and efficient review and supervision of research conducted in the United States. Veritas IRB is a US Department of Health and Human Services (DHHS) registered Independent Ethics Committee (#IRB00003814, #IRB00005916, #IRB00005917) and is constituted and operated according to the following US and international regulations and guidelines:.

mindprintsolutions.com mindprintsolutions.com

Mindprint Inc. CRO ERP/PSA Case Studies

http://www.mindprintsolutions.com/resources

CRO ERP / PSA Case Studies and other Resources. Please complete the below form and the below information will be emailed to you:. CRO Case Study: IMARC Research. CRO Case Study: Ockham Oncology. CRO Case Study: AlcheraBio LLC. CRO Case Study: ethica Clinical Research Inc. Webinar Slides: Slides presented at the Applied Clinical Trials webinar. Your Primary Interest *. 3601 Highway 7 East. Markham (Toronto), ON L3R 0M3. 2016 Created and Maintained by WSI.

veritasirb.com veritasirb.com

International Services

http://www.veritasirb.com/international-services/index.php

The Veritas IRB Difference. Veritas IRB is constituted for the review of studies in the United States and Canada. Established in 1996, Veritas IRB is one of the most experienced and respected research ethics boards in Canada, and we are the only central IRB to offer services to clients, sites and participants in English and French, Canada's two official languages. The Veritas IRB Difference. Ethica Clinical Research Inc.

ethicaclinical.com ethicaclinical.com

Independent Ethics Review

http://www.ethicaclinical.com/services/ethics-review.php

Assurance ⁄ Training. Clinical Quality Assurance / Training. Veritas IRB Inc. is an experienced and transparent Independent Review Board (IRB) committed to ensuring the safety, rights, and well-being of research participants. Clinical Quality Assurance and Training. Ethica Clinical Research Inc.

ethicaclinical.com ethicaclinical.com

Mission Statement

http://www.ethicaclinical.com/mission-statement

Assurance ⁄ Training. Ethica Clinical Research Inc. provides clinical study management, ethics review, quality assurance and DSMB services to sponsors of clinical research worldwide. We operate under the guiding principle that protecting the safety, rights and well-being of the human research participant is of paramount importance in all of our clinical research activities. Clinical Quality Assurance and Training. Ethica Clinical Research Inc.

ethicaclinical.com ethicaclinical.com

HISTORIC MILESTONE REACHED BY PHARMA OUTSOURCING COMPANY

http://www.ethicaclinical.com/CMS/index.php/8-press-room/66-historic-milestone-reached-by-pharma-outsourcing-company

Assurance ⁄ Training. HISTORIC MILESTONE REACHED BY PHARMA OUTSOURCING COMPANY. Ethica becomes the first privately-owned company to be accredited by Alion. Ethica selected Alion based on its long history of oversight, its practical approach to accreditation, and its commitment to continuous improvement of its accreditation standards. These attributes were validated during the accreditation process; Alion’s review was rigorous yet void of any unnecessary rigidity, according to Martin Letendre, Managin...

ethicaclinical.com ethicaclinical.com

Accreditation

http://www.ethicaclinical.com/accreditation

Assurance ⁄ Training. Ethica Clinical Research Inc. was founded on the principle that the protection of research participants and their rights should be of paramount importance to all organizations involved in the conduct and/or oversight of clinical research. Since its inception in 2002, ethica has been dedicated to ensuring that its processes respect participants' rights and that its services are delivered according to the highest standards of ethical and clinical practice. Ethica Clinical Research Inc.

ethicaclinical.com ethicaclinical.com

Services

http://www.ethicaclinical.com/services

Assurance ⁄ Training. Clinical Quality Assurance / Training. Ethica Clinical Research Inc. provides clinical study management, ethics review, quality assurance and DSMB services to sponsors of clinical research worldwide. We provide these services through our wholly-owned subsidiaries under the governance of our Human Research Protection Program (HRPP). Clinical Quality Assurance and Training. Ethica Clinical Research Inc.

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