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Dec 16


3-HOUR VIRTUAL SEMINAR ON EFFECTIVE CLEANING VALIDATION PROCEDURES

Part of the Lifesciences collection

3-Hour Virtual Seminar on Effective Cleaning Validation Procedures – Best
Practices

By Audiopence
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WHEN AND WHERE


DATE AND TIME

Fri, December 16, 2022, 1:00 PM – 4:00 PM EST


LOCATION

Online


REFUND POLICY

Contact the organizer to request a refund.


ABOUT THIS EVENT

 * 3 hours
 * Mobile eTicket


DESCRIPTION

This training program will be beneficial to personnel directly involved in the
development of cleaning procedures, cleaning validation programs and plans.
Additionally, those responsible for cleaning validation protocols and execution
activities, including validation and laboratory personnel, as well as, beginning
or seasoned operational personnel who will eventually participate in such
efforts, will find this course particularly useful.

This course will provide practical guidance on cleaning validation regulatory
compliance, in conjunction with, risk-based, reasonable and informed decision
making and activity planning. 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. Regulatory requirements
and the latest industry practices will also be included in the discussion.

Areas Covered in the Session :

 * FDA Requirements and Industry Standard Practices
 * How to Develop/Review Your Cleaning Procedures and the Adequate Selection of
   Cleaning Agents and Parameters
 * How to Develop a Cleaning Validation Policy/Program
 * How to Implement a Robust Cleaning Validation Plan
 * Laboratory Issues in Cleaning
 * Microbiological Aspects of a Cleaning Validation Program for Manufacturing
   Equipment
 * Keys to Cleaning Validation Maintenance – Remaining Compliant
 * Current FDA Concerns About Validation of Cleaning Processes

Who Should Attend:

 * Quality Departments
 * Engineering Departments
 * Production Departments
 * Manufacturing Departments
 * Validation Departments
 * Operations Departments
 * Process Owners
 * Quality Auditors

Additional service: (Personalized session)We also do various similar customized
events for our clients and it is specially tailored as per the client's
requirement. We arrange calls between clients and our course instructors to
better understand the training requirement and accordingly a training program is
designed. The course duration ranges between 90 Mins and 12 hours. Most 6 hours
and 12 hours of classes are split into 2 to 3 days considering customer
convenience.

We have 500+ consultants who are associated with us and each have their own
specialization example GxP, GMP,GLP, 21 CFR, Computer system validation, FDA
Audit & Inspection, Bioassays, Design Control, Data Integrity, FDA regulation,
Clinical compliance, and almost everything that falls under Risk, Quality and
Compliance arena in the Life Science industry.

If you think that your team needs some kind of boost, update or refresher in
Risk management and Regulatory compliance then let me know and we can design a
highly cost efficient program for you.

Personalized session please contact liz@theiqminds.com


TAGS

 * Online Events
 * Online Classes
 * Online Health Classes
 * #validation
 * #clinical
 * #laboratory
 * #clinicalresearch
 * #clinical_training
 * #laboratory_operations
 * #laboratory_research
 * #laboratory_management
 * #validation_documentation
 * #laboratory_analytics


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AUDIOPENCE

Organizer of 3-Hour Virtual Seminar on Effective Cleaning Validation Procedures



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$299 – $859
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