21 CFR, Parts 210 and 211

Поділитися
Вставка
  • Опубліковано 11 гру 2024

КОМЕНТАРІ • 11

  • @gustavopoueymirou-ortiz7981
    @gustavopoueymirou-ortiz7981 4 роки тому +1

    Excellent training. You got a 10 +

  • @joja2568
    @joja2568 2 роки тому

    Thank you. Very helpful!

  • @pharmamanu7
    @pharmamanu7 4 роки тому +1

    Lecture is clear and very useful,, Thank you Sir

  • @benseghirloundja7274
    @benseghirloundja7274 4 роки тому

    Great training thanks a lot.

  • @sakshigupta4177
    @sakshigupta4177 3 роки тому

    Very informative sir 🙏..... thanks

  • @curleyps6122
    @curleyps6122 4 роки тому +1

    thank you for the training
    though i have few questions
    may i know the exact difference between Batch and LOT
    what is in-process control
    would you suggest me how to obtain and remember all the 21cfr parts for GMP knowledge
    thank you

    • @thehealer8330
      @thehealer8330 3 роки тому

      What is the use ICH guidelines when 21 CFR already present? Sir plz give ur response. And how it corelate with each other?

  • @Trendingtubeforyou1
    @Trendingtubeforyou1 4 роки тому

    Very good thank u.

  • @sakshigupta4177
    @sakshigupta4177 3 роки тому +1

    Have you made a video on EC Principles of GMP (Directive 91/356/EEC) Article 6 to Article 14
    If not then please share your knowledge on the above topic 🙏..... waiting for your next session