Good Clinical Data Management Practices (GCDMP)

Date : 12th April 2018 to 13th April 2018

Place : United States, Philadelphia, pa

Website :https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901558SEMINAR?allconferencealerts-April-2018-SEO

Contact Person:Event Manager

Description:

Why should you attend: Good clinical data management (CDM) is paramount for a successful research. After all, Garbage In, Garbage Out (GIGO). CDM is involved in all aspects of collecting, processing, and interpreting information. There are many types of computer applications and database systems to support data collection and management. However, there are elements of Good Clinical Practice that apply across the board. Review and approval of drugs or devices by regulatory agencies requires the assumption that the data presented are valid and reliable. Integrity of the data is paramount to ensure confidence in the results and conclusions you will make. This seminar is based on FDA E6 GCP Guidelines which are the basis of effective data quality management. Even if your research is not FDA regulated, the information you learn in this course will help to ensure a robust data collection and management plan. The information conveyed in this course will also assist investigators in setting up processes for smoother data monitoring and auditing. Examples of CRF’s and required documentation will be presented. Data cleaning techniques will also be demonstrated. Additionally, this workshop will provide you with the knowledge and tools needed to assure GCDMP’s that hold up when the inevitable deviations from protocol occur. Who will benefit: Study Investigators Data managers Data processors Statisticians Site Personnel Clinical Research Associates Clinical Project Managers/Leaders Study Sponsors Professionals in pharmaceutical, medical device, clinical and biotechnology research who oversee or work with data collection and management Staff in the above fields who work with data collection/management and require training in GCDMP. Compliance auditors and regulatory professionals who require a knowledge of GCDMP in assessment of study protocols and reports Click to Continue Reading: https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901558SEMINAR?allconferencealerts-April-2018-SEO

Good Clinical Data Management Practices (GCDMP) will be held in Philadelphia, pa,United States on date 2018-04-13

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Deadline for abstracts/proposals : 11th April 2018

Keynote Speakers : Elaine Eisenbeisz, is a private practice statistician and owner of Omega Statistics, a statistical consulting firm based in Southern California. Elaine has over 30 years of experience in creating data and information solutions for industries ranging from governmental agencies and corporations, to start-up companies and individual researchers. In addition to her technical expertise, Elaine possesses a talent for conveying statistical concepts and results in a way that people can intuitively un

Conference Highlights :Study Investigators Data managers Data processors Statisticians Site Personnel Clinical Research Associates Clinical Project Managers/Leaders Study Sponsors Professionals in pharmaceutical, medical device, clinical and biotechnology research who oversee or work with data collection and management Staff in the above fields who work with data collection/management and require training in GCDMP.

Venue :Philadelphia, PA, USA

Check the event website for more details.