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Natural health products that inhibit angiogenesis : a potential source for investigational new agents to treat cancer - Part 2

by: shinta, 9 pages

The herbalist has access to hundreds of years of ob- servational data on the anticancer activity of many herbs. Laboratory studies are expanding the clinical knowledge that is ...

ETHICAL ISSUES IN THE DESIGN AND CONDUCT OF CLINICAL TRIALS IN DEVELOPING COUNTRIES

by: shinta, 4 pages

THERE has been considerable controversy about the ethics of clinical trials that are sponsored or conducted by groups in industrialized countries but carried out in developing ...

"Demystifying Clinical Trials"

by: Dan Sfera, 22 pages

Demystifying clinical trials in plain English. All you need to know if you are considering to join a clinical trial.

Informed Consent Sample "Treatment"

by: Dan Sfera, 16 pages

Sample Informed Consent. Should the word "treatment" be used?

GUIDANCE ON FDA REGULATORY REQUIREMENTS FOR INDIAN PHARMACEUTICAL INDUSTRY - Seminar By GlobalCOmpliancePanel

by: davidross759, 2 pages

Guidance on FDA Regulatory Requirements for Indian Pharmaceutical Industry 䀂 Approval process for FDA ٴ Submissions ٴ Process Validation ٴ Clinical Trials

Clinical Trials Strategy: The Clinical Development Plan

by: fadheela, 22 pages

Clinical Trials Strategy: The Clinical Development Plan

Information Security and Payment Card Rules: Protecting Patient Payment Data and Complying with PCI - Webinars By GlobalCompliancePanel

by: davidross759, 2 pages

Overview: In this session, attendees will learn what the PCI DSS requires for protection and how the PCI DSS relates to the HIPAA Security Rule - there are substantial similarities, and being ...

Key Elements of ICH-Q10 Pharmaceutical Quality System - Webinar By GlobalCompliancePanel

by: davidross759, 2 pages

Why you should attend: This webinar will help the participants understand what a Pharmaceutical Quality System is and how to transition from the compliance systems of today to the systems outlined in ...

Test Method Validation - The Characteristics - Webinar By GlobalCompliancePanel

by: davidross759, 2 pages

Overview: Although the concept of test method validation is based on good science, the expectation that test methods in the pharmaceutical industry be validated was established by the USP in the ...

Medical Device Classification - US and the EU as per MDD, CMDR and GHTF - Webinar By GlobalCompliancePanel

by: fazila, 2 pages

Medical Device Classification - US and the EU as per MDD, CMDR and GHTF - Webinar By GlobalCompliancePanel

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