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ENDPOINTECLINICAL.COM

EndPointe Clinical Resources, Inc.

Working with EndPointe Clinical. Phase 1 through Phase 4 Clinical Trials. Site Qualification, Study Operations Manual Development, and Team Training. Clinical Data Reviews and Medical Writing. Pre-Study Vendor Assessments, SOP Development, and Site Audits. Site Management, Vendor Management, and Clinical Monitoring. About EndPointe Clinical Resources. EndPointe provides clinical operations expertise to biotech and pharmaceutical organizations. Its founder, Elizabeth LaPointe. March 26, 2018. New targeted...

http://www.endpointeclinical.com/

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EndPointe Clinical Resources, Inc. | endpointeclinical.com Reviews
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Working with EndPointe Clinical. Phase 1 through Phase 4 Clinical Trials. Site Qualification, Study Operations Manual Development, and Team Training. Clinical Data Reviews and Medical Writing. Pre-Study Vendor Assessments, SOP Development, and Site Audits. Site Management, Vendor Management, and Clinical Monitoring. About EndPointe Clinical Resources. EndPointe provides clinical operations expertise to biotech and pharmaceutical organizations. Its founder, Elizabeth LaPointe. March 26, 2018. New targeted...
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2 clinical study management
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6 cardiology
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8 endocrinology
9 immunology and allergy
10 neurology
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EndPointe Clinical Resources, Inc. | endpointeclinical.com Reviews

https://endpointeclinical.com

Working with EndPointe Clinical. Phase 1 through Phase 4 Clinical Trials. Site Qualification, Study Operations Manual Development, and Team Training. Clinical Data Reviews and Medical Writing. Pre-Study Vendor Assessments, SOP Development, and Site Audits. Site Management, Vendor Management, and Clinical Monitoring. About EndPointe Clinical Resources. EndPointe provides clinical operations expertise to biotech and pharmaceutical organizations. Its founder, Elizabeth LaPointe. March 26, 2018. New targeted...

INTERNAL PAGES

endpointeclinical.com endpointeclinical.com
1

QA

http://endpointeclinical.com/wp/quality-assurance

Working with EndPointe Clinical. Phase 1 through Phase 4 Clinical Trials. Site Qualification, Study Operations Manual Development, and Team Training. Clinical Data Reviews and Medical Writing. Pre-Study Vendor Assessments, SOP Development, and Site Audits. Site Management, Vendor Management, and Clinical Monitoring. Standard Operating Procedures (SOPs):. Generation of a standard set of SOPs governing clinical activities. Assessments of SOP compliance and training. Staff Qualifications and Training Audits:.

2

About the Founder

http://endpointeclinical.com/wp/about-endpointe-clinical-resources/about-the-founder

Working with EndPointe Clinical. Phase 1 through Phase 4 Clinical Trials. Site Qualification, Study Operations Manual Development, and Team Training. Clinical Data Reviews and Medical Writing. Pre-Study Vendor Assessments, SOP Development, and Site Audits. Site Management, Vendor Management, and Clinical Monitoring. She left Lantheus to join AlloCure, Inc–a small biotech company that ran a Phase 2 program with allogeneic stem cells in the treatment of Acute Kidney Injury. Following the completi...Mutatio...

3

Working with EndPointe Clinical

http://endpointeclinical.com/wp/engaging-endpointe-clinical

Working with EndPointe Clinical. Phase 1 through Phase 4 Clinical Trials. Site Qualification, Study Operations Manual Development, and Team Training. Clinical Data Reviews and Medical Writing. Pre-Study Vendor Assessments, SOP Development, and Site Audits. Site Management, Vendor Management, and Clinical Monitoring. Working With EndPointe Clinical. EndPointe Clinical will provide a flexible contract to meet the ever-changing needs of the client. Please contact us. August 23, 2016. Early exposure to too m...

4

Documentation

http://endpointeclinical.com/wp/documentation

Working with EndPointe Clinical. Phase 1 through Phase 4 Clinical Trials. Site Qualification, Study Operations Manual Development, and Team Training. Clinical Data Reviews and Medical Writing. Pre-Study Vendor Assessments, SOP Development, and Site Audits. Site Management, Vendor Management, and Clinical Monitoring. Other document development services include:. Informed consent form template development. Clinical Trial Management Plans. Annual reports and PSURs. August 23, 2016. August 23, 2016. Nanofibe...

5

Training

http://endpointeclinical.com/wp/training-services

Working with EndPointe Clinical. Phase 1 through Phase 4 Clinical Trials. Site Qualification, Study Operations Manual Development, and Team Training. Clinical Data Reviews and Medical Writing. Pre-Study Vendor Assessments, SOP Development, and Site Audits. Site Management, Vendor Management, and Clinical Monitoring. To support this important area: EndPointe offers the following training services to our clients:. Protocol and Study Operations. Good Clinical Practice (focusing on sponsor responsibilities).

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EndPointe Clinical Resources, Inc.

Working with EndPointe Clinical. Phase 1 through Phase 4 Clinical Trials. Site Qualification, Study Operations Manual Development, and Team Training. Clinical Data Reviews and Medical Writing. Pre-Study Vendor Assessments, SOP Development, and Site Audits. Site Management, Vendor Management, and Clinical Monitoring. About EndPointe Clinical Resources. EndPointe provides clinical operations expertise to biotech and pharmaceutical organizations. Its founder, Elizabeth LaPointe. March 26, 2018. New targeted...

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