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Best Practices for Implementing an Effective Cleaning Validation

  February 12, 2018  
CfPA-The Center for Professional Advancement, Online Live
March 21, 2018 at 11:00 a.m.–12:30 p.m. (ET)

Who Should Attend?
This online training will benefit professionals in the Pharmaceutical, Biotechnology, and Medical Device Industries, who work as Quality Engineers, Validation Engineers, Managers, Supervisors, Operators, Analysts, Auditors, and Chemists in departments such as Manufacturing, Quality Control and Quality Assurance, and Engineering, as well as Research and Development. 

Course Description
This highly interactive course brings online training to a new, enhanced level with open discussions and direct feedback to the instructor throughout the presentation. The training will include participant discussions with shared examples of their laboratory issues and bioburden issues. This 90-minute, accredited training course provides practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable and informed decision making and activity planning. The course will describe the requirements for establishing an effective cleaning validation program, including the development of a general policy, cleaning SOPs and other appropriate documentation. In addition, participants will understand the requirements for maintaining a validated cleaning process. 

Can't Make this LIVE Webinar? 
Simply select the On Demand option when registering and we will send you the link to view the recorded version.

This course will be available On Demand: March 22, 2018
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
   Joy McElroy, Consultant to the pharmaceutical and biotech industries

With 10 years of experience as a consultant, and over 20 years total experience in the pharmaceutical and biotech industries, Ms. McElroy has gained extensive knowledge of Quality Assurance, Process and Cleaning Validation, and Equipment Qualification. She has written and executed Equipment Qualification and Validation Protocols for numerous Companies. Ms. McElroy specializes in Equipment Qualification, Sterilization, Cleaning Validation, and GMP Compliance Auditing. In 2013 Ms. McElroy started her own company, Maynard Consulting Company, which provides top engineers, auditors, and validation specialist to pharmaceutical, biotech and medical device clients worldwide.
Deadline for Abstracts: n/a
Registration: Please click here for registration information.
E-mail: jmorbit@cfpa.com
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