About Regulatory Requirements Cleaning Validation 2018
Regulatory Requirements Cleaning Validation 2018 will be opened on 08 Mar and it will be ended on 09 Mar 2018.
Regulatory Requirements Cleaning Validation 2018 will take place at the Hilton Zurich Airport in Zurich, Switzerland.
Regulatory Requirements Cleaning Validation 2018 is regarded as an exciting Course which will cover the topics of Pharmaceutical, Biotechnology, Cleaning Validation and Cleaning Procedures and far more.
Regulatory Requirements Cleaning Validation 2018 is organized three times a year.
The organizer of the Regulatory Requirements Cleaning Validation 2018, Regulatory Requirements Cleaning Validation | FDA Guidelines 2018 is Global Compliance Panel.
Let Zurich must do holiday attractions make you fall in love with this city when you are there for Regulatory Requirements Cleaning Validation 2018. Here are the top notch things to do in Zurich!
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. The program will describe the requirements for establishing an effective cleaning validation program, including the development of a general policy, a "Cleaning Validation Master Plan" and the appropriate documentation for each study to be performed. In addition, requirements for maintenance of the validated status will be reviewed.
Important Dates
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 manufacturing equipment
Lecture 3: Keys to Cleaning Validation Maintenance - Remaining Compliant Lecture 4: Current FDA concerns about validation of cleaning processes
Leave Your Comment