This seminar is designed to acquaint all Participants with the Rules and Regulations that form the background of what is know as the GCP of Clinical Research. To follow The Good Clinical Practices (GCP) is to follow the standard for the design, conduct, performance, monitoring, auditing, recording, analysis and reporting of clinical trails that provides assurance that the data and reported results are credible and accurate and, most importantly, that the safety, rights, integrity, and confidentiality of trial subjects is protected. That all members of the team must know and practice GCP guarantees, that the Protocol is followed, that the Informed

Date : 2nd November 2017 to 3rd November 2017

Place : United States, Baltimore, md

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901348SEMINAR?allconferencealerts-November-2017-SEO

Contact Person:Eevnt Manager

Description:

This seminar is designed to acquaint all Participants with the Rules and Regulations that form the background of what is know as the GCP of Clinical Research. To follow "The Good Clinical Practices" (GCP) is to follow the standard for the design, conduct, performance, monitoring, auditing, recording, analysis and reporting of clinical trails that provides assurance that the data and reported results are credible and accurate and, most importantly, that the safety, rights, integrity, and confidentiality of trial subjects is protected. That all members of the team must know and practice "GCP" guarantees, that the Protocol is followed, that the Informed

This seminar is designed to acquaint all Participants with the Rules and Regulations that form the background of what is know as the GCP of Clinical Research. To follow The Good Clinical Practices (GCP) is to follow the standard for the design, conduct, performance, monitoring, auditing, recording, analysis and reporting of clinical trails that provides assurance that the data and reported results are credible and accurate and, most importantly, that the safety, rights, integrity, and confidentiality of trial subjects is protected. That all members of the team must know and practice GCP guarantees, that the Protocol is followed, that the Informed will be held in Baltimore, md,United States on date 2017-11-03

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Deadline for abstracts/proposals : 1st November 2017

Keynote Speakers : Charles H Pierce, MD, PhD, FCP, CPI From an original Master's thesis (MSc in Pharmacology) in 1961 (Minnesota) through a Doctorate in Surgery-Pharmacology in 1974 (Saskatchewan) and continuing throughout 48+ years in the practice of clinical medicine as a family physician (7 years as an ER doc) and 28+ years in the medical research industry (7 years as a Principal Investigator), Charles has an experienced based knowledge of the Clinical Research part of Drug Development. He is an APPI/AP

Conference Highlights :This lecture series will provide invaluable assistance to industry study sponsors and those involved in Setting up the IND to follow the regulatory / legal responsibilities and also the ethical considerations in pharmaceutical product (IMP) research involving human subjects. Those benefiting the most would be: The Study Sponsor Principal Investigators and sub investigators Clinical Research Scientists (PKs, Biostatisticians, ...) Safety Nurses Clinical Research Associates (CRAs) and Coordin

Venue :Baltimore, MD, United States

Check the event website for more details.