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Clinical Research Jobs in India, USA, Europe, Japan, Singapore, UK, etc.Discussions related to clinical research jobs and career. 

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Bioavailability and Bioequivalence
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Pharmacovigilance
Pharmacovigilance (PV) is the pharmacological science relating to the detection, assessment, understanding and prevention of adverse effects

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Since outsourcing of Clinical Trials by Pharmaceutical and biotech companies is increasing by the day, this board will help to increase knowledge and understanding in this subject

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Laboratory Discussions
Reference Labs, Bioanalytical Labs, Good Lab Practices, Assay Troubleshooting, Reference Ranges and other discussions

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Statisticians, statistical programmers and medical writers can discuss issues important to them here. Also includes data management. Courses in Data Management

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Investigator Site Staff
Principal Investigator, Co-Investigator, Sub-Investigator, Coordinator, and other site staff can discuss issues related to them here. Courses for PI and CRC inside.

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Clinical Research Associates (CRAs) can discuss the various aspects of their day to day happenings - monitoring, travel, audits, report writings, and everything else...

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Discuss the revolutionary concepts of drug development from bench to bedside and vice versa. Courses in Translational Medicine.

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Anything that doesn't fit anywhere else should be discussed here. Strictly clinical research only.

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Resources

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Discuss Clinical Research Courses and Training Programs. Find free training resources. Rate Colleges and Online Clinical Research Programs.

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Resources related to clinical research
Articles, Videos, Audio Lectures, Podcasts, Useful Links, Online Clinical Research Course demos, Course Videos

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Ethics in Clinical Research

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Discussions related to Ethics
Ethical considerations have a variety of roles in clinical trials - from matters related to the design of a study, to the conduct and even to the reporting of results

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International conference on Harmonization and Good Clinical Practice
The ICH brings together the regulatory authorities of Europe, Japan and the United States and experts from pharmaceutical industry to discuss scientific and technical aspects of product registration

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Informed Consent in Clinical Research Studies
Discuss guidelines, regulations and issues related to Informed consent process for clinical trials

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General Category

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You will find periodic announcements here

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