Conference Details

This 2 day course will cover practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable and informed decision making and activity planning. This two day interactive course will cover fundamental principles of a cleaning validation program, exploring such concepts as the determination of residues to be targeted, selection of analytical and sampling methods, determination of appropriate limits in various pharmaceutical and biotechnology processes, and establishment of scientific rationales acceptable to regulatory inspectors.

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Place : United States, Washington d.c.

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Contact Person:Event Manager

Description:

This 2 day course will cover practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable and informed decision making and activity planning. This two day interactive course will cover fundamental principles of a cleaning validation program, exploring such concepts as the determination of residues to be targeted, selection of analytical and sampling methods, determination of appropriate limits in various pharmaceutical and biotechnology processes, and establishment of scientific rationales acceptable to regulatory inspectors.

This 2 day course will cover practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable and informed decision making and activity planning. This two day interactive course will cover fundamental principles of a cleaning validation program, exploring such concepts as the determination of residues to be targeted, selection of analytical and sampling methods, determination of appropriate limits in various pharmaceutical and biotechnology processes, and establishment of scientific rationales acceptable to regulatory inspectors. will be held in Washington d.c.,United States on date 2016-06-03

Deadline for abstracts/proposals : 31st May 2016

Organized By :NetZealous LLC - GlobalCompliancePanel

Keynote Speakers : conference on Cleaning Validation Program,development of cleaning procedures, best practices for cleaning validation programs and plans,Cleaning Validation Master Plan,Requirements for Establishing an Effective Cleaning Validation Program,fundamental principles of a cleaning validation program

Conference Highlights : Agenda: Day 1 Schedule: Lecture 1: • FDA Requirements and Industry Standard Practices Lecture 2: • How to Develop/Review your Cleaning Procedures and the Adequate Selection of Cleaning Agents and Parameters Lecture 3: • How to Develop a Cleaning Validation Policy/Program Lecture 4: • How to Implement a Robust Cleaning Validation Plan Day 2 Schedule: Lecture 1: • Laboratory Issues in Cleaning Lecture 2: • Microbiological aspects of a cleaning validation program for

Venue :Washington, D.C., DC, United States

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This 2 day course will cover practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable and informed decision making and activity planning. This two day interactive course will cover fundamental principles of a cleaning validation program, exploring such concepts as the determination of residues to be targeted, selection of analytical and sampling methods, determination of appropriate limits in various pharmaceutical and biotechnology processes, and establishment of scientific rationales acceptable to regulatory inspectors.

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