An SOP is a meticulous step-by-step description of how to do a task that leave no chance for errors and divergence. Writing a good SOP is not an easy job. It requires a firm understanding of the task to be described, an ability to describe in specific unique to that laboratory. Writing, implementing, maintaining and assessing, revising an SOP are all different and necessary jobs. Many people must continuously be involved in these steps. Even a standardized method, such as an ASTM or IP method, is insufficiently written to pass as a well-written and compliant SOP. Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900914SEMINAR?allconferencealerts_SEO

Date : 8th June 2017 to 9th June 2017

Place : United States, Baltimore

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900914SEMINAR?allconferencealerts_SEO

Contact Person:Eevnt Manager

Description:

An SOP is a meticulous step-by-step description of how to do a task that leave no chance for errors and divergence. Writing a good SOP is not an easy job. It requires a firm understanding of the task to be described, an ability to describe in specific unique to that laboratory. Writing, implementing, maintaining and assessing, revising an SOP are all different and necessary jobs. Many people must continuously be involved in these steps. Even a standardized method, such as an ASTM or IP method, is insufficiently written to pass as a well-written and compliant SOP. Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900914SEMINAR?allconferencealerts_SEO

An SOP is a meticulous step-by-step description of how to do a task that leave no chance for errors and divergence. Writing a good SOP is not an easy job. It requires a firm understanding of the task to be described, an ability to describe in specific unique to that laboratory. Writing, implementing, maintaining and assessing, revising an SOP are all different and necessary jobs. Many people must continuously be involved in these steps. Even a standardized method, such as an ASTM or IP method, is insufficiently written to pass as a well-written and compliant SOP. Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900914SEMINAR?allconferencealerts_SEO will be held in Baltimore,United States on date 2017-06-09

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Deadline for abstracts/proposals : 6th June 2017

Keynote Speakers : John C. Fetzer, has had over 30 year experience in HPLC methods development. He has authored or co-authored over 50 peer-reviewed papers on liquid chromatography, has served on the editorial advisory boards of the Journal of Chromatography, Analytical Chemistry, and Analytical and Bio analytical Chemistry.

Conference Highlights :Research Associates Lab Chemists Lab Supervisors Quality Officers

Venue :Baltimore, MD, United States

Check the event website for more details.