How to decide the concentration for the sample and standard in related substances?

Sdílet
Vložit
  • čas přidán 26. 04. 2021
  • How to set the concentration for the sample and standard in related substances?
    More than 1000+ pharma professionals have chosen Pharma Growth Hub as their career acceleration partner, now it’s your turn!
    27 courses worth Rs. 1,16,690/- are available for just Rs. 6990/- This offer may not stay for long, so take action.
    Please find the main module details below...
    1. Assay method validation mastery
    » Everything you need to know to perform assay validation
    » Preparation of conc. matrix, protocol, calculations, report wrt global requirements
    2. Dissolution method validation mastery
    » Everything you need to know to perform dissolution validation
    » Preparation of conc. matrix, protocol, calculations, report wrt global requirements
    3. Related substances method validation mastery
    » Everything you need to know to perform RS validation
    » Preparation of conc. matrix, protocol, calculations, report wrt global requirements
    4. Residual Solvents method validation mastery
    » Everything you need to know to perform Res sol. validation
    » Preparation of conc. matrix, protocol, calculations, report wrt global requirements
    5. Extractables & Leachables Blueprint
    » What is E&L
    » What is the source of E&L
    » How to use Risk-based approach for safety assessment
    » What are Thresholds for E&L
    » How to design E&L Study
    6. Stability Study Mastery
    » Basic terms in stability study
    » Stability study for submission
    » Preparation of stability protocol, report
    » IQ, OQ,PQ of stability chamber
    7. Method development blueprint
    » HPLC, GC, Dissolution, Spectroscopy Method Development
    8. Cleaning validation blueprint
    » How to perform cleaning validation
    9. Mutagenic & Nitrosamines
    » Understand regulatory aspects of mutagenic & nitrosamines
    » Testing need of Mutagenic & Nitrosamine into your product
    » LOQ requirement for Nitrosamine test procedure
    » Limit for new Nitrosamine impurity
    » Limit for mutagenic impurity
    10. QMS Mastery
    » Incident, OOS, OOT, CAPA, Change control
    » QMS examples
    11. ICH Quality Blueprint
    » Comprehensive course on ICH Quality guidelines
    12. FDA 483 Observations
    » Comprehensive info on FDA 483 recd. By Indian Pharma (10-12 yrs)
    13. Impurity Management blueprint
    » Limit for known, unknown, total impurity
    » Limit for residual solvents
    » Release & Stability specification for Impurity
    14. Instrument Calibration Mastery
    » Calibration of common lab instrument
    » Calibration templates & formats
    15. Instrument Qualification mastery
    » Qualification of common lab instruments
    » Calibration templates & formats
    16. Information Technology Blueprint
    » Electronic data management
    » Server Data Backup, Retrieval, and Verification
    » Preparation, Execution & Review of CSV
    17. Specification design blueprint
    » Specification for API/Finished product
    » Specification for unknown impurity
    » Specification for known impurity
    18. Pharma tech blueprint
    » More than 90+ videos on various topics of QC, QA, AR&D
    19. Concentration matrix design mastery
    » Concentration matrix for method validation
    » Confirmation on selected weighing and dilution details
    » Mapping expected concentrations for API/Impurities
    20. Calculation formula design mastery
    » Reporting and rounding of analytical results
    » Basic calculation functions in excel
    » Basic calculation formulas in Analytical chemistry
    » Preparation of automated calculation sheet
    21. Concentration design blueprint
    » Conc. Optimization for assay, RS, Dissolution, Residual solvent
    22. Lab Operation Blueprint
    » Basic Lab Set-Up Guidance
    23. Interview Question Model
    » Likely Interview Questions
    24. Job Search Strategy
    » 3 Month job search plan
    » Job search tracker
    » How to connect with TAMs
    » How to communicate with TAM
    25. Resume & LinkedIn Blueprint
    » Resume optimization
    » LinkedIn optimization
    » Resume writing
    » Converting resume templates
    26. Job interview blueprint
    » Job interview checklist
    » Job INTERVIEW questions
    » Phrases to avoid
    » Power of words
    27. Inner circle calls
    » Previously recorded sessions
    » Opportunity to network with PGH Stars
    Payment link (Rs.6990): imjo.in/vPe7Rc
    Alternate payment options(GPay/PhonePe): 9766383968
    WhatsApp @9766383968 for more info…

Komentáře • 62

  • @rajunaikbadhavath3442
    @rajunaikbadhavath3442 Před 3 lety +2

    yours videos are highly appreciable and useful...thank you lot

  • @huteshbharambe8558
    @huteshbharambe8558 Před 3 lety +7

    Plz make video on "How to develop method from a given molecular structure"

  • @durgalavanya7037
    @durgalavanya7037 Před 2 lety

    Very worthable vedio to me. Tq sir.. Please educate like this way with more vedios

  • @lvramirdy84
    @lvramirdy84 Před 2 lety

    Cleary understood ....how to set standard and sample concertration... Thank you.........

  • @ingisproduction8072
    @ingisproduction8072 Před 2 lety

    Thanks Sir, it's new for me. Thanks for upgrading....

  • @harikrishnareddybhumireddy4198

    ur explanation is very good thanks sir

  • @radhakrishna8186
    @radhakrishna8186 Před 4 měsíci

    Hi Bhaskar sir, this is the first ever channel which is providing enormous knowledge to our pharma professionals. God bless you and your family 👌❤

  • @achyutjagdhane9683
    @achyutjagdhane9683 Před 3 lety +1

    thank you , it is very helpful

  • @bhausahebhingade3541
    @bhausahebhingade3541 Před 3 lety

    Thanks sir very good keep it up work

  • @arunvishwakarma5109
    @arunvishwakarma5109 Před 11 měsíci

    Thank you very much sir for such support

  • @sathishkorumilli6064
    @sathishkorumilli6064 Před 2 lety

    very good explaination sir

  • @sravanthithota8951
    @sravanthithota8951 Před 2 lety

    Sir thanku for ur valuable information

  • @subratmishra6468
    @subratmishra6468 Před 2 lety

    It's nice explaination..

  • @bharathivendhan
    @bharathivendhan Před 3 lety +1

    Easy understanding

  • @sachinsawant6932
    @sachinsawant6932 Před 3 lety +2

    Sir, your all vedios are knowledgeable and helpful 🙏🙏

  • @jitendratarmale6310
    @jitendratarmale6310 Před 2 lety +1

    Very helpful

  • @shekhargoud3964
    @shekhargoud3964 Před 2 lety

    Good videos sir..

  • @basavarajuraju323
    @basavarajuraju323 Před 2 lety

    Thank you sir it's nice vedeo

  • @bandikattuvenkatasiva2542

    Thank you so much sir

  • @rupchandpitekar3772
    @rupchandpitekar3772 Před 2 lety

    Thank you for describe

  • @balajiorchid
    @balajiorchid Před 2 lety +5

    Dear sir, First of all thanks for helping me to improve the knowledge. In this class I have one small doubt sir, I am not understand to set the concentration of standard clearly sir

    • @remborathod-ry2bx
      @remborathod-ry2bx Před 9 měsíci

      Standard concentration is set according to the specifications of the highest unknown specifications impurity for eg. Unknown impurity specifications are 0.2% and sample concentration is 1000ppm simply cross multiplication we will get standard concentration.

  • @prasadmallavarapu7740
    @prasadmallavarapu7740 Před 2 lety

    Thank you sir

  • @NaushadAlam-vs9ij
    @NaushadAlam-vs9ij Před 3 lety

    Very good

  • @sagarsatbhai
    @sagarsatbhai Před 2 lety +1

    Pls mk vdo on how to rectify process and degrade impurity if possible. Thnk you!!

  • @srinivaschintha9958
    @srinivaschintha9958 Před rokem

    I am hapy to you,thank you very much sir,your vedio was very useful for whom studying drug analysis by HPLC
    Sir i need to how to calculate for LOD and LOQ in both sample and standard drug and formulation using HPLC with perfectly
    Thank you sir

  • @vinodpatil9202
    @vinodpatil9202 Před 2 lety

    Great

  • @abhishekjoshi9650
    @abhishekjoshi9650 Před 2 lety

    Thank u sir

  • @lovehindustan710
    @lovehindustan710 Před rokem

    Thank you

  • @pharmagrowthhub3083
    @pharmagrowthhub3083  Před 2 lety

    💊How to develop skill set to advance your career📈 in QA, QC, AR&D💊
    Join me online on SUNDAY, 1st Aug between 7:00 pm to 9:00 pm to learn below
    ✔4 steps to build technical competency in QA, QC, AR&D 💥💥
    ✔3 pillars to reach your full potential 🚀🚀
    ✔3 strategies to influence your marketplace 🤩🤩
    Free Webinar Registration link: us02web.zoom.us/webinar/register/7616276120910/WN_5nss-f3ETuaJ4lr_BzrPBQ
    Join WhatsApp Group: chat.whatsapp.com/HB5rP5P1rgy62fT8FgNBlS
    I look forward to meet you inside room

  • @rahulkulkarni3037
    @rahulkulkarni3037 Před 2 lety

    Perfect

  • @shankarsharma2822
    @shankarsharma2822 Před 3 lety

    Thanks

  • @RazaKhan-ds8by
    @RazaKhan-ds8by Před 2 lety +1

    where 1ppm come from and how did find SN 10. please not clear

  • @tadalavenkateswararao2090

    Sir why prepared std concentration in unknown level? And why must be our reporting threshold with inthe

  • @sutraina2474
    @sutraina2474 Před 2 lety +1

    Sir how to fix limit for dissolution of tablets or capsules dosage forms???

  • @Mukesh-ne3yj
    @Mukesh-ne3yj Před 2 lety

    Nice

  • @pimaop2553
    @pimaop2553 Před 3 lety

    sir I need to know use of buffer compostion and its pH? WITH SOLVENT

  • @amirkhusru4603
    @amirkhusru4603 Před rokem

    informative

  • @harishasnayak5249
    @harishasnayak5249 Před 3 lety

    Good video
    Please make video on RS qualifications techniques

  • @abhishekjoshi9650
    @abhishekjoshi9650 Před 2 lety

    Pl make different video of method development Related Substance..

  • @vijaykumar-md2xk
    @vijaykumar-md2xk Před 3 lety +1

    Very well explained

    • @pharmagrowthhub3083
      @pharmagrowthhub3083  Před 3 lety

      Glad it was helpful!

    • @dils2678
      @dils2678 Před 2 lety

      @@pharmagrowthhub3083sir.... requesting you to make vedio on Analytical method development
      Reply sir

  • @buddepumohanarao8309
    @buddepumohanarao8309 Před 3 lety

    Excellent sir

  • @gopalgirase-01
    @gopalgirase-01 Před rokem

    Sir, What is chart purity?

  • @gopalgirase-01
    @gopalgirase-01 Před 11 měsíci

    How decide sample conc in assay?

  • @tadalavenkateswararao2090

    Sir why taken standard concentration higher unknown impurity %

  • @Bhavisyacreations2019
    @Bhavisyacreations2019 Před rokem +1

    Sir, Can you elaborate how 1ppm = 0.025 percentage
    I think that is 25 ppm right

    • @harikrishnanayyappan9179
      @harikrishnanayyappan9179 Před 9 měsíci

      There is very simple calculation,
      Impurity LOQ in % /100 × Sample Concentration in ppm = Impurity in ppm
      0.025/100× 4000= 1ppm,
      Note: above calculation I used 100 because your Impurity LOQ in %, hence
      Example:
      Assay in % : mg per mL / Labled Amount × 100 = content in %

  • @Mukesh-ne3yj
    @Mukesh-ne3yj Před 2 lety

    RS sple concentration in API afyer method set

  • @AliRaza-wp8tr
    @AliRaza-wp8tr Před rokem

    Can somebody tell me how 1ppm equals to 0.025%

  • @SG73088
    @SG73088 Před 2 lety +1

    Sir, please take lecture on isolation of impurities by Preparative HPLC and it's profile topic.

  • @Aaakashkaushik
    @Aaakashkaushik Před 2 lety

    Sir plz translate in hindi

  • @NaushadAlam-vs9ij
    @NaushadAlam-vs9ij Před 2 lety +1

    Sir you can't explain proper