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PARTICIPANT REGISTRATIONJoint EFGCPAREC Workshop on Research Ethics Committee Difficult Cases 26 February 2008, Brussels, BelgiumPlease use BOLD LETTERS or TYPE and return this form to: EGGCUP Secretariat
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Start by downloading the joint efgcp-arec workshop registration form from the official website.
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Who needs joint efgcp-arec workshop on?

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The joint efgcp-arec workshop is beneficial for individuals and organizations involved in clinical research and ethics.
02
Researchers and scientists who conduct clinical trials and need to stay updated with the latest regulatory guidelines and ethical considerations.
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Clinical trial sponsors who want to ensure compliance with international standards and improve their processes.
04
Ethics committee members who review and approve research protocols, ensuring protection of participants' rights and welfare.
05
Healthcare professionals involved in clinical research, including doctors, nurses, and pharmacists.
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Hospital administrators and research coordinators responsible for managing clinical trials.
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Regulatory authorities and policymakers who need to stay informed about advancements and challenges in clinical research.
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Professionals working in contract research organizations (CROs) and pharmaceutical companies.
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Academic institutions and universities involved in medical and scientific research.
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Overall, anyone interested in gaining knowledge and exchanging experiences related to ethical considerations in clinical research can benefit from this workshop.

What is Joint EFGCP-AREC Workshop on Research Ethics Committee Difficult Cases Form?

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The joint efgcp-arec workshop focuses on discussing ethical and regulatory aspects of clinical trials.
Researchers, sponsors, and ethics committee members are required to file joint efgcp-arec workshop.
The joint efgcp-arec workshop can be filled out online or submitted via email following the provided guidelines.
The purpose of the joint efgcp-arec workshop is to ensure compliance with ethical standards and regulations in clinical research.
The joint efgcp-arec workshop must include details of the clinical trial protocol, informed consent process, and monitoring procedures.
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