Continued Process Verification

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  • เผยแพร่เมื่อ 2 ก.พ. 2024
  • #pharmaceutical #csv #csa #validation #quality #qrm #riskmanagement #fda #compliance #gmp #ich
    This session will make you understand the "Continued Process Verification" requirements in line with the various guideline expectations for example - EUGMP, FDA, WHO guide etc.
    The agenda for this session is as below;
    Understanding Continuous Process Verification - Importance, Need and Purpose
    Know your Trainer
    Difference between ‘Product Quality Review’ and ‘Continuous Process Verification’
    Guideline Requirements - USFDA, EU, WHO etc.
    Difference between USFDA and EU Regulations for Process Validation
    Role of Continued Process Verification in process validation and its practical implementation
    FDA Citations on Continued Process Verification
    Q&A
    Vote of Thanks and contact details
    Subscribe - / @hitendrakumarshah3718
    Link for webinar of Process validation - Regulatory and Practical View - th-cam.com/users/live_0NDBOVfjHk?...
    Link for FDA guideline for process validation - www.fda.gov/regulatory-inform...
    Link Process Validation - Key Questions and Answers 1 - • Process Validation - K...
    Link Process Validation - Key Questions and Answers 2- • Process Validation - K...
    Join this channel to get access to perks:
    / @hitendrakumarshah3718
  • วิทยาศาสตร์และเทคโนโลยี

ความคิดเห็น • 12

  • @balvinderkumar5383
    @balvinderkumar5383 4 หลายเดือนก่อน +2

    Appreciate sir, and thank you
    Keep uploading informated and valuable videos...request to do on stratified sampling also...

  • @sonikumar7269
    @sonikumar7269 หลายเดือนก่อน

    Thank u very much Sir ji for valuable information. I have question related to data point. As u suggested 20 data point. Please help for details information related 20 data points with example for better clarity.

  • @masthangm4836
    @masthangm4836 3 หลายเดือนก่อน +1

    Very comprehensively the subject is elaborated, thanking indeed. Can we not use the data collection from PQR to establish process stability as they are intra batch data? In spite of ongoing program. Please advise.

    • @masthangm4836
      @masthangm4836 3 หลายเดือนก่อน +1

      Because, all CQA and CPP data are collected to demonstrate the process stability.

    • @masthangm4836
      @masthangm4836 3 หลายเดือนก่อน +1

      ​@@sarvilsanavBro! I have mentioned PQR which is Product Quality Review not PPQ! 😊

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  3 หลายเดือนก่อน

      The data from PQR can be used to evaluate process capabiilty and not process stability.

    • @masthangm4836
      @masthangm4836 3 หลายเดือนก่อน

      Thanks alot Sir! 👌👍

  • @Bharatpithiyalive
    @Bharatpithiyalive 4 หลายเดือนก่อน +2

    Sir... Kindly share link of FDA guidelines

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  4 หลายเดือนก่อน

      I have uploaded all relevant links in description section.

  • @prashantpandey668
    @prashantpandey668 4 หลายเดือนก่อน +1

    Need presentation