3-Hour Virtual Seminar on Effective Cleaning Validation Procedures

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