.

Key Factors to Write an Effective Standard Operating Procedure 2017 Baltimore

Thu, November 2 - Fri, November 3, 2017 Linthicum Heights, Maryland
DoubleTree by Hilton Baltimore - BWI Airport 890 Elkridge Landing Rd Linthicum Heights, Maryland 21090 United States +1 410-859-8400

About Key Factors to Write an Effective Standard Operating Procedure 2017 Baltimore

KEY FACTORS TO WRITE AN EFFECTIVE STANDARD OPERATING PROCEDURE, BALTIMORE, NOVEMBER 02-03, 2017

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. The reasons why will be described, as will the steps needed to convert a standard method into an SOP.

The necessary steps both within the laboratory and within the supporting areas for implementation and revision of an SOP are complex and will be described. These include recordkeeping, safety, training, and other areas.

This event will take place at DoubleTree by Hilton Baltimore - BWI Airport,890 Elkridge Landing Rd, Linthicum Heights, Maryland.

Who will benefit:

Anyone that creates / maintains SOPs

VP, Director, Manager of any dept that writes SOPs or performs training

QA / QC

Regulatory Affairs

Why should you attend:

A poorly written and followed SOP is one of the most common non-compliances that an auditor finds. If you are a laboratory worker, a supervisor, or manager of a laboratory seeking or under GLP or ISO 17025, you should know how to create and maintain a good SOP. Will your SOPs pass an audit or will they become a non-compliance corrective action?

About Key Factors to Write an Effective Standard Operating Procedure 2017 Baltimore

KEY FACTORS TO WRITE AN EFFECTIVE STANDARD OPERATING PROCEDURE, BALTIMORE, SEPTEMBER 21-22, 2017

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. The reasons why will be described, as will the steps needed to convert a standard method into an SOP.

The necessary steps both within the laboratory and within the supporting areas for implementation and revision of an SOP are complex and will be described. These include recordkeeping, safety, training, and other areas.

Who will benefit:

  • Anyone that creates / maintains SOPs
  • VP, Director, Manager of any dept that writes SOPs or performs training
  • QA / QC
  • Regulatory Affairs

Why should you attend:

A poorly written and followed SOP is one of the most common non-compliances that an auditor finds. If you are a laboratory worker, a supervisor, or manager of a laboratory seeking or under GLP or ISO 17025, you should know how to create and maintain a good SOP. Will your SOPs pass an audit or will they become a non-compliance corrective action?

About Key Factors to Write an Effective Standard Operating Procedure 2017 Baltimore

KEY FACTORS TO WRITE AN EFFECTIVE STANDARD OPERATING PROCEDURE, BALTIMORE, SEPTEMBER 21-22, 2017

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. The reasons why will be described, as will the steps needed to convert a standard method into an SOP.

The necessary steps both within the laboratory and within the supporting areas for implementation and revision of an SOP are complex and will be described. These include recordkeeping, safety, training, and other areas.

This event will take place at DoubleTree by Hilton Baltimore - BWI Airport, 890 Elkridge Landing Rd, Linthicum Heights, Maryland.

Who will benefit:

  • Anyone that creates / maintains SOPs
  • VP, Director, Manager of any dept that writes SOPs or performs training
  • QA / QC
  • Regulatory Affairs

Why should you attend:

A poorly written and followed SOP is one of the most common non-compliances that an auditor finds. If you are a laboratory worker, a supervisor, or manager of a laboratory seeking or under GLP or ISO 17025, you should know how to create and maintain a good SOP. Will your SOPs pass an audit or will they become a non-compliance corrective action?

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