Канал: PharmaTED

ICH Q9 Quality Risk Management || QRM || @PharmaTED

ICH Q9 Quality Risk Management || QRM || @PharmaTED

ICH Q8 Pharmaceutical Development || @PharmaTED

ICH Q8 Pharmaceutical Development || @PharmaTED

Process Validation: General Principles and Practices || @PharmaTED

Process Validation: General Principles and Practices || @PharmaTED

Change to an Approved NDA and ANDA || Reporting Category For Industry || @PharmaTED

Change to an Approved NDA and ANDA || Reporting Category For Industry || @PharmaTED

SUPAC-MR: Modified Release || Extended Release || Delayed Release || @PharmaTED

SUPAC-MR: Modified Release || Extended Release || Delayed Release || @PharmaTED

SUPAC-IR: Immediate Release Solid Oral Dosage Form || Full Guidelines || @PharmaTED

SUPAC-IR: Immediate Release Solid Oral Dosage Form || Full Guidelines || @PharmaTED

Crospovidone || Why CrosPovidone used in Tablets and Capsules || Excepients @PharmaTED

Crospovidone || Why CrosPovidone used in Tablets and Capsules || Excepients @PharmaTED

Ethanol || Why Ethanol used in Binder Solution || Excepients @PharmaTED

Ethanol || Why Ethanol used in Binder Solution || Excepients @PharmaTED

Polysorbate 80 || Binder Solution || Why Polysorbate 80 used in Tablets || @PharmaTED

Polysorbate 80 || Binder Solution || Why Polysorbate 80 used in Tablets || @PharmaTED

Why Povidone Used In Tablets || Binder Solution || Excepients || @PharmaTED

Why Povidone Used In Tablets || Binder Solution || Excepients || @PharmaTED

Why Croscarmellose Sodium In Tablets || Excepients || @PharmaTED

Why Croscarmellose Sodium In Tablets || Excepients || @PharmaTED

Why Sodium Chloride Used In Tablets || Excepients || @PharmaTED

Why Sodium Chloride Used In Tablets || Excepients || @PharmaTED

Why Mannitol Used In Tablets || Excepients || @PharmaTED

Why Mannitol Used In Tablets || Excepients || @PharmaTED

Why Used Microcrystalline Cellulose In Tablets || Excepients || @PharmaTED

Why Used Microcrystalline Cellulose In Tablets || Excepients || @PharmaTED

21 CFR - General Information || @PharmaTED

21 CFR - General Information || @PharmaTED

How many titles in CFR || @PharmaTED

How many titles in CFR || @PharmaTED

21 CFR Available in how many Languages || @PharmaTED

21 CFR Available in how many Languages || @PharmaTED

Types of Capsules Size || Capsule Size | @PharmaTED

Types of Capsules Size || Capsule Size | @PharmaTED

Calibration of Balance || Balance Calibration || USP chapter 1251 || USP Chapter 41 @PharmaTED

Calibration of Balance || Balance Calibration || USP chapter 1251 || USP Chapter 41 @PharmaTED

Calibration of Disintegration Test Apparatus || USP Chapter-701 || @PharmaTED

Calibration of Disintegration Test Apparatus || USP Chapter-701 || @PharmaTED

Calibration of Friability Test Apparatus || USP Chapter 1216 || @PharmaTED

Calibration of Friability Test Apparatus || USP Chapter 1216 || @PharmaTED

Calibration of Moisture Analyzer || Loss of Drying || Part of USP chapter 731 @PharmaTED

Calibration of Moisture Analyzer || Loss of Drying || Part of USP chapter 731 @PharmaTED

Stage - 3 Continuous Process Verification || Process Validation-CPV | @PharmaTED

Stage - 3 Continuous Process Verification || Process Validation-CPV | @PharmaTED

Stage -2 Process Qualification || Process Validation Stage -2 PQ || @PharmaTED

Stage -2 Process Qualification || Process Validation Stage -2 PQ || @PharmaTED

Stage -1 Process Design || Process Validation || @PharmaTED

Stage -1 Process Design || Process Validation || @PharmaTED

Process Validation - Regulatory Requirements || @PharmaTED

Process Validation - Regulatory Requirements || @PharmaTED

Process Validation - Approach || Approach of Process Validation @PharmaTED

Process Validation - Approach || Approach of Process Validation @PharmaTED

Process Validation - Introduction and Background | Pharmaceutical Industries | @PharmaTED

Process Validation - Introduction and Background | Pharmaceutical Industries | @PharmaTED

Qualification Of Vendor | RM And PM In Pharmaceutical Companies | @PharmaTED

Qualification Of Vendor | RM And PM In Pharmaceutical Companies | @PharmaTED

Tablet Friability Test || Apparatus, Procedure, Calibration @PharmaTED

Tablet Friability Test || Apparatus, Procedure, Calibration @PharmaTED

Disintegration Test || Apparatus, Procedure, Calibration @PharmaTED

Disintegration Test || Apparatus, Procedure, Calibration @PharmaTED

Time Frame Of Field Alert Report @PharmaTED

Time Frame Of Field Alert Report @PharmaTED

Where Do I Submit Field Alert Report @PharmaTED

Where Do I Submit Field Alert Report @PharmaTED

If I do not Submit Field Alert Report @PharmaTED

If I do not Submit Field Alert Report @PharmaTED

Form 3331a For Submitting Field Alert Report @PharmaTED

Form 3331a For Submitting Field Alert Report @PharmaTED

Who is Responsible for submission of Field Alert Report @PharmaTED

Who is Responsible for submission of Field Alert Report @PharmaTED

FAR - Field Alert Report Submission Required if Racall is initiated @PharmaTED

FAR - Field Alert Report Submission Required if Racall is initiated @PharmaTED

FAR- Field Alert Report Submission For Root Cause Identity of Distributed Products @PharmaTED

FAR- Field Alert Report Submission For Root Cause Identity of Distributed Products @PharmaTED

FAR - Field Alert Report Submission For Media Fill Failure @PharmaTED

FAR - Field Alert Report Submission For Media Fill Failure @PharmaTED

FAR - Field Alert Report Submission For OOS Result For Distributed Products @PharmaTED

FAR - Field Alert Report Submission For OOS Result For Distributed Products @PharmaTED

FAR - Field Alert Report Submission for OOS Result For Not Distributed Products @PharmaTED

FAR - Field Alert Report Submission for OOS Result For Not Distributed Products @PharmaTED

FAR - Field Alert Report Submission For Other Markets @PharmaTED

FAR - Field Alert Report Submission For Other Markets @PharmaTED

FAR Submission For Packing or Components @PharmaTED

FAR Submission For Packing or Components @PharmaTED

Criteria For Submission of FAR - Field Alert Report @PharmaTED

Criteria For Submission of FAR - Field Alert Report @PharmaTED

Consideration of Significant Changes For Submission of FAR - Field Alert Report @PharmaTED

Consideration of Significant Changes For Submission of FAR - Field Alert Report @PharmaTED

Initial FAR, Followup FAR AND Final FAR || Field Alert Report Submission @PharmaTED

Initial FAR, Followup FAR AND Final FAR || Field Alert Report Submission @PharmaTED

What is FAR - Field Alert Report || FAR Submission @PharmaTED

What is FAR - Field Alert Report || FAR Submission @PharmaTED

FAR-Field Alert Report || For Distributed Drug Product # 21 CFR 314.81 (b) (1) @PharmaTED

FAR-Field Alert Report || For Distributed Drug Product # 21 CFR 314.81 (b) (1) @PharmaTED

Leak Test # In Pharmaceutical Packing @PharmaTED

Leak Test # In Pharmaceutical Packing @PharmaTED

Laboratory Control General Requirement || 21 CFR Subpart - I 211.160 (a) @PharmaTED

Laboratory Control General Requirement || 21 CFR Subpart - I 211.160 (a) @PharmaTED

Pharmacode || Packing component Control System @PharmaTED

Pharmacode || Packing component Control System @PharmaTED

Principle of GS1- System || GS1 Standard Use @PharmaTED

Principle of GS1- System || GS1 Standard Use @PharmaTED

Pharmaceutical Coding || GS1 - General Specification || Barcode Coding || 2D Coding @PharmaTED

Pharmaceutical Coding || GS1 - General Specification || Barcode Coding || 2D Coding @PharmaTED

GS1- General Specification Introduction | GS1 System Introduction @PharmaTED

GS1- General Specification Introduction | GS1 System Introduction @PharmaTED

Penicillin Contamination || As Per 21CFR 211.176 @PharmaTED

Penicillin Contamination || As Per 21CFR 211.176 @PharmaTED

Stability Testing || As Per 21 CFR 211.166 @PharmaTED

Stability Testing || As Per 21 CFR 211.166 @PharmaTED

Reserve Sample || Control Sample | 21 CFR 211.170 @PharmaTED

Reserve Sample || Control Sample | 21 CFR 211.170 @PharmaTED

Difference Between 21 CFR 210 And 211 || 21 CFR @PharmaTED

Difference Between 21 CFR 210 And 211 || 21 CFR @PharmaTED

New Product Development || Drug Product @PharmaTED

New Product Development || Drug Product @PharmaTED

NPI || New Product Introduction || Drug Product @PharmaTED

NPI || New Product Introduction || Drug Product @PharmaTED

Management Notifications || In Pharmaceutical Companies @PharmaTED

Management Notifications || In Pharmaceutical Companies @PharmaTED

OOT || Out Of Trend in Pharmaceutical industry @PharmaTED

OOT || Out Of Trend in Pharmaceutical industry @PharmaTED

OOS || Out Of Specifications in Pharmaceutical industry @PharmaTED

OOS || Out Of Specifications in Pharmaceutical industry @PharmaTED

CAPA || Corrective And Preventative Action @PharmaTED

CAPA || Corrective And Preventative Action @PharmaTED

PRODUCT RECALL || Pharmaceutical Product Recall @PharmaTED

PRODUCT RECALL || Pharmaceutical Product Recall @PharmaTED

Market Complaint || Of Pharmaceutical Products @PharmaTED

Market Complaint || Of Pharmaceutical Products @PharmaTED

Deviation || PNC/MNC @PharmaTED

Deviation || PNC/MNC @PharmaTED

CHANGE CONTROL || In Pharmaceutical Industries @PharmaTED

CHANGE CONTROL || In Pharmaceutical Industries @PharmaTED

QUALITY MANUAL (QM) | ICH Guidelines | @PharmaTED

QUALITY MANUAL (QM) | ICH Guidelines | @PharmaTED

Validation Master Plan (VMP) | VMP In Pharmaceutical industry | @PharmaTED

Validation Master Plan (VMP) | VMP In Pharmaceutical industry | @PharmaTED

Site Master File |SMF For Regulatory Submission @PharmaTED

Site Master File |SMF For Regulatory Submission @PharmaTED

ICH Q1 A Stability Testing | ICH Guidelines | @PharmaTED

ICH Q1 A Stability Testing | ICH Guidelines | @PharmaTED

Photostability Testing || ICH Q1B Stability Testing @PharmaTED

Photostability Testing || ICH Q1B Stability Testing @PharmaTED

Stress Testing || ICH Q1A Stability Guidelines @PharmaTED

Stress Testing || ICH Q1A Stability Guidelines @PharmaTED

Pharmaceutical Audits @PharmaTED || Types of Pharmaceutical Audits.

Pharmaceutical Audits @PharmaTED || Types of Pharmaceutical Audits.

Pharmacopoeia || Regulatory Pharmacopoeia Definition, History @PharmaTED

Pharmacopoeia || Regulatory Pharmacopoeia Definition, History @PharmaTED

Pharmaceutical Regulatory Agencies|| @PharmaTED

Pharmaceutical Regulatory Agencies|| @PharmaTED

CAPA || Corrective And Preventative Action | @PharmaTED

CAPA || Corrective And Preventative Action | @PharmaTED

Process Capability (CpK) | @PharmaTED

Process Capability (CpK) | @PharmaTED

APQR || APQR/APR/PQR @PharmaTED

APQR || APQR/APR/PQR @PharmaTED

NDA/ANDA || Reporting Categories For Post Approval Changes @PharmaTED

NDA/ANDA || Reporting Categories For Post Approval Changes @PharmaTED

SUPAC-IR || In Vivo Bioequivalence Study/Documentations @PharmaTED

SUPAC-IR || In Vivo Bioequivalence Study/Documentations @PharmaTED

SUPAC-IR || In Vitro Dissolution @PharmaTED

SUPAC-IR || In Vitro Dissolution @PharmaTED

SUPAC-IR || Dissolution Testing @PharmaTED

SUPAC-IR || Dissolution Testing @PharmaTED

SUPAC-IR || Dissolution Testing ( Pooled Sample) | @PharmaTED

SUPAC-IR || Dissolution Testing ( Pooled Sample) | @PharmaTED

SUPAC-IR || Dissolution testing @PharmaTED

SUPAC-IR || Dissolution testing @PharmaTED

SUPAC-IR || Scale-Up and Scale-Down 02 @PharmaTED

SUPAC-IR || Scale-Up and Scale-Down 02 @PharmaTED

SUPAC-IR || General Information | @PharmaTED

SUPAC-IR || General Information | @PharmaTED

RMG (Rapid Mixture Granulator)|| Used in Pharmaceutical companies @PharmaTED

RMG (Rapid Mixture Granulator)|| Used in Pharmaceutical companies @PharmaTED

STIRRER || Used in Pharmaceutical Companies For Granulation Process | @PharmaTED

STIRRER || Used in Pharmaceutical Companies For Granulation Process | @PharmaTED

PASTE PREPARATION VESSELS ||Used in Pharmaceutical companies | @PharmaTED

PASTE PREPARATION VESSELS ||Used in Pharmaceutical companies | @PharmaTED

VIBRO SIFTER USED IN PHARMACEUTICAL COMPANIES FOR GRANULATION PROCESS | @PharmaTED

VIBRO SIFTER USED IN PHARMACEUTICAL COMPANIES FOR GRANULATION PROCESS | @PharmaTED

DISPENSING BOOTH USED IN PHARMACEUTICAL COMPANIES | @PharmaTED

DISPENSING BOOTH USED IN PHARMACEUTICAL COMPANIES | @PharmaTED

AIR LOCK SYSTEM IN PHARMACEUTICAL INDUSTRIES | @PharmaTED

AIR LOCK SYSTEM IN PHARMACEUTICAL INDUSTRIES | @PharmaTED

UNIFORMITY AS PER (IP/BP/USP) LIMIT | @PharmaTED

UNIFORMITY AS PER (IP/BP/USP) LIMIT | @PharmaTED

M.Pharma in Quality Assurance (QA) Department!!RGPV University!!

M.Pharma in Quality Assurance (QA) Department!!RGPV University!!

BANSAL COLLEGE OF PHARMACY !! BANSALOTSHAV 2017 !!

BANSAL COLLEGE OF PHARMACY !! BANSALOTSHAV 2017 !!

BANSAL COLLEGE OF PHARMACY !! , STAR BATCH 2014 -2018

BANSAL COLLEGE OF PHARMACY !! , STAR BATCH 2014 -2018

Paras ka patthar

Paras ka patthar

Creative Ashish Vishwakarma

Creative Ashish Vishwakarma