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Pharma Scholars
India
เข้าร่วมเมื่อ 12 ก.ย. 2020
5S JAPANESE TECHNIQUES (@PharmaScholars )
The 5S method is a cyclical methodology for improving work environments that uses five steps, or "pillars", to create a more organized and productive workspace.
#5S_METHODOLOGY
#WHAT_IS_5S
#5S_KYA_hota_he
#5s_kya_he
#5s_kise_khte_hain
#Seiri
#SEITON
#SEISO
#SEIKETSU
#SHITSUKE
#BENEFITS_OF_5S
#5S_IN_HINDI_EASY_EXPLANATION
#5S_JAPNESE_TECHNIQUE
#IMPORTANCE_OF_5S
#5s_in_hindi_video
#5s_in_hindi_with_example
#5s_meaning_in_hindi
#5s_safety_in_hindi
#5s_training_in_hindi
#5s_slogan_in_hindi
#5s_in_ayat
#5S_METHODOLOGY
#WHAT_IS_5S
#5S_KYA_hota_he
#5s_kya_he
#5s_kise_khte_hain
#Seiri
#SEITON
#SEISO
#SEIKETSU
#SHITSUKE
#BENEFITS_OF_5S
#5S_IN_HINDI_EASY_EXPLANATION
#5S_JAPNESE_TECHNIQUE
#IMPORTANCE_OF_5S
#5s_in_hindi_video
#5s_in_hindi_with_example
#5s_meaning_in_hindi
#5s_safety_in_hindi
#5s_training_in_hindi
#5s_slogan_in_hindi
#5s_in_ayat
มุมมอง: 20
วีดีโอ
Sanitization of Water Systems(@PharmaScholars )
มุมมอง 34หลายเดือนก่อน
SANITIZATION:- Microbial control in water systems is achieved primarily through sanitization practices. Systems can be sanitized using either thermal or (photo-) chemical means. THERMAL SANITIZATION:- Thermal approaches to system sanitization include periodic or continuously circulating hot water and the use of steam. #Santisation_of_Purified_Water_System #Sanitisation_of_water_system_Easy_expl...
Water System Validation As per USP
มุมมอง 78หลายเดือนก่อน
Validation is the process to demonstrate that the design and operation of a pharmaceutical water system consistently produces water that meets USP requirements. USP General Chapter 1231 provides extensive discussion of the life cycle elements to maintain a validated state of control. #th-cam.com/video/ladNGz5vQJE/w-d-xo.html #Water_System_validation_in_Pharmaceitical_industry #Water_system_qual...
MACO CALCULATIONS(@PharmaScholars )
มุมมอง 2852 หลายเดือนก่อน
One of the key parameters in cleaning validation is the maximum allowable carryover (MACO), which is the amount of residue that can be transferred from one product to another without compromising quality, safety, or efficacy. MACO can be calculated using different methods, such as 10 ppm, Dose based, and health-based #MACO_CALCULATIONS #Maximum_Allowable_Carryover #PPM_Method_criteria_maco_calc...
Standard Operating Procedures(SOP) (@PharmaScholars )
มุมมอง 833 หลายเดือนก่อน
Standard Operating Procedures (SOPs) are an integral part of the day-to-day operations in the pharmaceutical industry, and every department must have its own SOPs. (@PharmaScholars ) #SOP #SOP_IN_HINDI #SOP_EASY_EXPLANATION #STANDARD_OPERATING_PROCEDURE_IN_PHARMA_INDUSTRY #SOP_EXPLANATION #EXPLAIN_SOP #SOP_IN_PRODUCTION #SOP_IN_QUALITY_ASSURANCE #SOP_IN_PLANT #SOP_IN_PHARMACEUTICALS #SOP_IN_PHA...
New Dosage Form Stability Testing (ICH Q1C)(@PharmaScholars )
มุมมอง 903 หลายเดือนก่อน
#New_dosage_form_stability_study #New_dosage_form_stability_testing #ICH_Q1C #New_dosage_form_Expiry_date #New_dosage_form_drug_development
PHOTO STABILITY STUDY (@PharmaScholars )
มุมมอง 523 หลายเดือนก่อน
The ICH guideline Q1B for photostability testing gives guidance on the basic testing protocol required to evaluate the light sensitivity and stability of new drugs and products. The choice of the irradiation method, although complying with the guideline demands, may effect test results. High irradiances may shorten testing times, but can lead to enforcement of photodegradation, which was demons...
#ICH_Stability_Guidelines_For_New_Drug_Products_and_Substances ( @PharmaScholars )
มุมมอง 763 หลายเดือนก่อน
#ICH_GUIDELINES_Q1(R2) #ICH_GUIDELINES_FOR_NEW_PRODUCTS_AND_SUBSTANCES #ICH_STABILITY_GUIDELINES_FOR_NEW_SUBSTANCES_AND_NEW_PRODUCTS #LONG_TERM_STABILITY #REAL_TIME_STABILITY_STUDY #Accelarted_stability_study #short_term_stability_study #intermediate_stability_study #Ich_stability_zones #ICH_stabilty_testing_guidelines #Ich_guidelines_q1_principle #schedule_P #Forced_degradation_study_ich_guide...
Alcoa_in_English(@PharmaScholars )
มุมมอง 343 หลายเดือนก่อน
ALCOA is a set of principles that ensures data integrity in the life sciences sector. It was introduced by, and is still used by, the FDA - the US Food and Drug Administration. It has relevance in a range of areas, particularly in relation to pharmaceutical research, manufacturing, testing, and the supply chain. As well as being crucial for compliance reasons, ALCOA principles are becoming incr...
ICH GUIDELINES (@PharmaScholars )
มุมมอง 1213 หลายเดือนก่อน
The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is unique in bringing together the regulatory authorities and pharmaceutical industry to discuss scientific and technical aspects of drug registration. Since its inception in 1990, ICH has gradually evolved, to respond to the increasingly global face of drug development. ICH's mission i...
Worst case identification in cleaning validation (@PharmaScholars )
มุมมอง 2083 หลายเดือนก่อน
The selection of the “worst case” scenario in cleaning validation embodies a critical risk assessment phase, targeting the effective removal of all residues - including active ingredients, excipients, and cleaning agents - to forestall cross-contamination or microbial growth in subsequent manufacturing cycles. This encompasses a dynamic range of strategies from choosing potent cleaning agents t...
ROLES_AND_RESPONSIBILITIES_OF_QUALITY CONTROL (@PharmaScholars )
มุมมอง 383 หลายเดือนก่อน
ROLES_AND_RESPONSIBILITIES_OF_QUALITY CONTROL QC_department_work_in_pharmaceutical_companies QC_department_work_in_pharmaceutical_industry Qualifications_for_QC_DEPARTMENT Works_of_quality_control_department quality_control_department_me_kya_kaam_krte_hain QC_department_me_kya_kaam_krte_hain QC_department_me_kya_kaam_krna_pdta_he (@PharmaScholars )
Role_of_qa_in_pharma_industry (@PharmaScholars )
มุมมอง 423 หลายเดือนก่อน
QA in the pharmaceutical industry involves implementing systems and processes to ensure that products consistently meet or exceed established quality standards. It encompasses activities such as Good Manufacturing Practices (GMP), quality management systems, and adherence to regulatory requirements. #Role_of_qa_in_pharma_industry #qa_role_in_pharma_industry #Qa_work_in_Pharma_industry #Quality_...
#Quality_Risk_Management (Pharma Scholars)
มุมมอง 533 หลายเดือนก่อน
The Food and Drug Administration (FDA or Agency) is announcing the availability of a final guidance for industry entitled “Q9(R1) Quality Risk Management.” The guidance was prepared under the auspices of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH). The guidance is a targeted revision of the 2006 guidance for industry “Q9 Quality ...
SCOPE OF PHARMACY (@PharmaScholars )
มุมมอง 313 หลายเดือนก่อน
First and foremost, the major benefit of choosing Pharmacy would be the high employment rates. According to a study, only 1.3% of the people with a Degree in Pharma are unemployed. According to the data for 2021, the total number of job openings was 13,600 and it is predicted that it will reach the inclined end of the graph in the future. Pharmacy as a subject has been ranked under the top 20 p...
IIT DELHI HOSPITAL PHARMACIST (@PharmaScholars )
มุมมอง 1113 หลายเดือนก่อน
IIT DELHI HOSPITAL PHARMACIST (@PharmaScholars )
DRUG INSPECTOR VACANCIES (@PharmaScholars )
มุมมอง 593 หลายเดือนก่อน
DRUG INSPECTOR VACANCIES (@PharmaScholars )
GOVT. PHARMA VACANCIES (@PharmaScholars )
มุมมอง 523 หลายเดือนก่อน
GOVT. PHARMA VACANCIES (@PharmaScholars )
GENERIC MEDICINES DARK SIDE (@PharmaScholars )
มุมมอง 1.3K3 หลายเดือนก่อน
GENERIC MEDICINES DARK SIDE (@PharmaScholars )
GRANULATION STAGE 10 MOST IMPORTANT INTERVIEW QUESTIONS(@PharmaScholars )
มุมมอง 884 หลายเดือนก่อน
GRANULATION STAGE 10 MOST IMPORTANT INTERVIEW QUESTIONS(@PharmaScholars )
TOP 10 INTERVIEW QUESTIONS IN PHARMA INDUSTRY (@PharmaScholars )
มุมมอง 705 หลายเดือนก่อน
TOP 10 INTERVIEW QUESTIONS IN PHARMA INDUSTRY (@PharmaScholars )
Calculation of Related Substances By Percentage Normalisation Method (@PharmaScholars )
มุมมอง 625 หลายเดือนก่อน
Calculation of Related Substances By Percentage Normalisation Method (@PharmaScholars )
PROCESS VALIDATION- A NEW APPROACH (@PharmaScholars )
มุมมอง 1465 หลายเดือนก่อน
PROCESS VALIDATION- A NEW APPROACH (@PharmaScholars )
CRITICAL PROCESS PARAMETERS (CPP) & CRITICAL QUALITY ATTRIBUTES (CQA) (@PharmaScholars )
มุมมอง 7627 หลายเดือนก่อน
CRITICAL PROCESS PARAMETERS (CPP) & CRITICAL QUALITY ATTRIBUTES (CQA) (@PharmaScholars )
DEVIATION FORM FILLING IN PHARMA(@PharmaScholars )
มุมมอง 2488 หลายเดือนก่อน
DEVIATION FORM FILLING IN PHARMA(@PharmaScholars )
DEVIATION IN PHARMACEUTICAL INDUSTRY(@PharmaScholars )
มุมมอง 5908 หลายเดือนก่อน
DEVIATION IN PHARMACEUTICAL INDUSTRY(@PharmaScholars )
Calibration of Moisture Analyser (@PharmaScholars )
มุมมอง 3109 หลายเดือนก่อน
Calibration of Moisture Analyser (@PharmaScholars )
PACKING VALIDATION IN PHARMA (@PharmaScholars)
มุมมอง 35110 หลายเดือนก่อน
PACKING VALIDATION IN PHARMA (@PharmaScholars)
A critical point very easy explained
Very informative Vedeo learning for CV
Watch other videos also. They will be so helpful to you.
Yes sir @@PharmaScholars
if u wiil explain with practically in excel its much better for understand
Very well explained sir ..
Thanks for the compliment
Very good information
Very simple way understanding for a critical point of CV
Thanks for the compliments.
Best vdo
Thank you for your compliment.
Please explains change control risk assessment, impact assessment and action items for change in excipient, API vendor Change in equipment Change in area Change in location / site Introducing new product Change in batch size Change in software
Sure
Very helpful information sirjii
Calculation bhi karate to accha rahta
Good one. Need more details
Thank you❤
Welcome dear
Nice
Thanks for your compliment
Really good
Thanks for your compliment
Nice
Thanks
Nice
Thanks
Nice video thanx
You are welcome
Good 👍 awesome
Thanks for your compliment dear
Good explanation brother keep it up
Thanks for your compliment
Sir minor defect kitne percent chal sakta hai ,?
@Madhubala Minor defect limit is NMT 4% .
@@PharmaScholars sir formula kya hai tablet capsule sample pick krne ka
@@MadhuBala-tl1dr Go through ISO guidelines 2859-01
Go through Guidelines ISO 2859-01
Good sir...tq
Welcome dear
Thanks 🙏 sir for making this.
You are welcome dear ❤
Excellent work. Thanks a lot 🙏🌹🙏
So nice of you
Well explained
Thanks Hemant for your compliment 😊
Thanks mam ji
Nice explained
Thanks ❤compliment
Sir I am understand very well 😊
Thanks for the compliment. Keep supporting dear 💕
🔥
😞 *promosm*
0:38 Granulation 1:53 Importance of Granulation 4:18 Types of Granulation 5:16 End point of Granulation 6:43 RMG 7:10 Principle of RMG 8:23 Methods to determine powder flow 8:49 Mesh No. 9:44 Kneading time 10:27 Critical Process Parameters & Critical Quality Attributes at Granulation stage
Very useful❤
Glad to hear that
Easy for learning simple way explained
Sir, Why 0.41 using and where it omes from
This is a standard factor given by USP.
Air regularly video dala kro maine aapki sari videos dekhi hai
Thanks g. Keep supporting the channel 🙏😊
@@PharmaScholars sure sir I have suggestion for you Aap shorts bhi dala kro aapkay efforts ka acha result aayega
Great suggestion. I will surely implement this.
4:00 tablet capping 8:41 Dwell time 14:02 Tablet Lamination 17:24 Tablet Sticking 20:00 Tablet Picking
Well explained
Thanks dear
Thank you sir
Welcome g
What is dwell time and kneeding time
For Dwell time please watch tablet defects part-1.th-cam.com/video/l3ax5eWJgAM/w-d-xo.htmlsi=G9xO2x2ElIdP41gM
Thanks for making this Video.. It's good
You are welcome dear ☺☺☺
Awesome 👍
Thanks for compliment 🤗
Nice 👍👍 awesome
Thanks for the visit
wah kya baat
Tnq sir
Which guideline we use for water validation? Is which bases how we design phase III schedule
guidelines I have mentioned in the description box. You can check it out.
Please make video on related substances and it's calculation
Sure dear. I am going to make a video🎥 on this topic soon.
Plse share file of this video again
Very nice❤❤
Many many thanks
Good sir can you explain qualifications of hvac system from urs to pq.
sir please explain properly
Ok mam. Please tell me what didn't you understand.
Try upcoming videos in English
Sure dear 👍
Thanks sir Ek melting point ki bi bna do
Sure dear 👍