MAY 12, 2020 9:00 AM PDT

Analytical Quality Control for the Pharmaceutical Industry

Sponsored by: Sartorius
C.E. Credits: P.A.C.E. CE Florida CE
Speaker
  • Owner and Consultant, McElroy Training and Consultancy, LLC
    Biography
      Upon earning a degree in Zoology at North Carolina State University, Joy began working in the pharmaceutical and biotech industries in 1992 at Pharmacia & UpJohn performing Environmental Monitoring and Sterility Testing. Her work allowed her to move into a supervisory role at Abbott Laboratories where she oversaw the Quality Control Lab. In 1998 Joy moved to Wyeth Lederle and worked in Quality Assurance, performing GMP Compliance audits, batch record reviews, and holding annual GMP training for new employees. After working in Quality Assurance for a few years, Joy moved into Equipment Qualification and Cleaning Validation at Mallinckrodt.
      With 19 years of experience as a consultant, and over 25 years total experience in the pharmaceutical and biotech industries, Joy has gained extensive knowledge of Quality Assurance, Technical Writing, Process and Cleaning Validation, and Equipment Qualification and Computer System Validation and Part 11 Compliance. She has written and executed Equipment Qualifications and Validation Protocols for numerous Companies such as Mallinckrodt, Wyeth Lederle, Merck, BioMerieux, Catalent, and Biotest, Novartis, Imprimis, Cody Laboratories, and Xceilence.
      Her knowledge and experience, have made her a highly sought-after engineer, technical writer, and trainer in both the pharmaceutical and biotech industries. Joy specializes in Equipment Qualification, Cleaning Validation, and GMP Compliance Auditing, and technical writing, and GMP, Audit Preparation, and SOP writing training, Computer System Validation and Part Compliance.
      In 2019 she opened her own company, McElroy Training and Consultancy, LLC which provides consultants for various projects as well as on and off - site training to pharmaceutical and biotech companies throughout the United States.
      Joy also spends her time mentoring and speaking as an Empowerment Speaker. Her goal is to empower people all over the world to live their dreams though implementing 5 simple techniques she has learned and applied through the years.

    Abstract
    This webinar, previously set for April 23rd has been rescheduled to: 
     
    DATE:  May 12, 2020
    TIME:   9:00am PDT, 12:00pm EDT

    Analytical quality control refers to all those processes and procedures designed to ensure that the results of laboratory analysis are consistent, comparable, accurate and within specified limits. Quality control begins with sample collection and ends with the reporting of data. It is achieved through laboratory control of analytical performance.

    This presentation will discuss Analytical Quality Control for pharmaceuticals as it relates to pipetting, weighing, sample collection and preparation, as well as analytical method and equipment qualification.

    We will examine best practices to provide thoughts and ideas to develop or improve the performance of your current system. This presentation will help attendees understand the instrument qualification and system validation process and will provide instruction on how to prepare for audits and how to become FDA compliant.

     

    Webinars will be available for unlimited on-demand viewing after live event.
     
    LabRoots is approved as a provider of continuing education programs in the clinical laboratory sciences by the ASCLS P.A.C.E. ® Program. By attending this webinar, you can earn 1 Continuing Education credit once you have viewed the webinar in its entirety.


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