GMP Pharmaceutical guidelines for Good Manufacturing Practices (GMP) Manufacturing Practices, Therefore, do vis this page regulary. + Regulatory Guidelines on Data Integrity + Stops to Minimize the Data Integy Risk + Toa Qually Management (TOM) + EDA Waning Letters far leaning Validation + Identification of Worst Gase in Cleaning Validation + Bull a Qualty Culture in Pharmaceuticals + Conitol of Contamination a Diferent Manufacturing Stages + Computerized System Valalion Planting and Exacution + Validation Program in Pharmaceutical Industies ‘+ Quatty Marual and Qualty Potcy + Diference between Gener and Branded Medici + Difference Between HEPA and ULPA Filters + Implementation of Six Sigma in the Pharmaceutical Industry + Lean Six Sigma Concent + Data ntesatyin Mcrabial Analysis + Importance of Data Integy in Pharmaceuticals + Basics of Cleaning Validation + Alois and Change Rooms in oGMP Facity + Periodic Review and Compliance in the Pharmaceutical Indu + Beduce Vallaion Gost in Pharmacautcals ‘+ Resuicements and implementation of Continuous Training in Pharmaceuticals + Citra for Selection of Clean Room Garments in Phavmy + Planning and Execution of Internal Audits in Pharmacoutea + Requirements and Mainlonance of HVAC System in Manufacturing Facies + Why Gold Chain Logistics are Requled in Pharmaceuticals? + Difference between cGMP and GMP + Difference between GMP ang GLP + Validation ofthe Etfectivenass of UV Lightin Water System + Besuicements ol FDA for rainngin Pharmacauticals + How to Sta a Phamaceutical Formulation Plant? + Difeonce Between Dynamic and Static Pass ox + Guidlines for Drug Master Fle Submission + Environmental Risk from Microbial Waste + Different Tyoes of Hand Disinfectants Used in Pharmaceuticals Different Tyoes of Chemical Indicators for Steiiztion on tn arenapietn or published on this blog. This page updates when we wile an article on Good‘+ (Checklist for Audit in Purchase Department + Drug Mastar Fil and Types of OME + USEDA Audit Points! Observations + Bracketing and Matixing n Pharmaceutical Stabilty + Blasimiaes and thei Sinficance in Pharm + Bast Weighing Practoss in Pharmacsutca + Princile and Working of Fludzed Bed Dryer (EBD) + Requirement of Active and Passive Ar Sampling in Contoled Areas “+ 2L.CER and Its Recommendations + Fishbone Tool of investigation in Pharmaceuticals blems Assos teal Cl + Possbiies ofc vion in Storia P + ALCOA in Pharmaceuticals A necessary tol for Quaty + Importance of Negative and Postive Controls in Mcrabal Analysis + Various Types of Blenders and Thelr Purpose + Performance Qualification (PO) of Pharmaceutical Ea with Pharmace room Areas + Concept of GAMP 5 in Pharmaceuticals 2 for Tolophanie In + 5 Tipe Interview io Pharmaceuticals + GLP in Mezobislogy Laboratory + Enviconmentallolates and Ther Library in Stele Pharmaceuticals + Concept af GxP in Pharmaceuticals + Epoxy Flooring and lis Benefits in Pharmaceuticals + Difforonce belwoen Fumigation and Feoging + How to Propare for a EDA Ingpacton + Process Analiial Technology (PAT) in Pharmaceuticals + Quality by Design (QbD) in Pharmaceuticals + Quality Management System (QMS) + Importance and Method of De-cassing in Putiied Water System 3108 of Validation in Pharma ti + tmpar + Handling Static Charge in Pharmacautcal Manufacturing + \mpovtance of Qualified Parsans in Pharmaceuticals ‘+ \mportance of Blend Uniformly in Manufacturing Process + Wy Fins Must Avoid FDA 489 and Warning Lelters? ‘+ Requirements for Good Documentation Pu + Acceptable Qualty Level (AQL) in Pharmaceuticals + Prooedure for Sampling in Process Validation + 1s-Fungal Count Acceptable in Pharmaceutical Classified Area? + Ways to Reduce Human Eros in Pharmaceuticals n of Ar Changes per Hour in Clean Room Area + Validation of Fumigation in Cleanroom A + Importance ane Maintenance of Pressure Dilferentialin Manufacturing Area, + Besuirement of Alanm System in Clical Equements ‘+ How Effectively Exacute a Validation Protocol? + GMP for Stone hy teal Manufacturing + Depyrogenation in Inaction Manufacturing + Containers for Pnarmaceutical Packasing + Calculation for Capacity of Tablet Coating Machine + Sanitation in Pharmaceutical Manufacturing + Working and Principle of Tablet Caatiog Machine + Isolalors and Their Use in Stele Manufacturing + Working and Prncile of Collada! Mi + Working and Principle of Ragid Mixer Granulator (MG) + Common Ways to Avoid the Most Frequent GMP Evrors Look for during EDA Inspaction? Data integrity Issues Found During Inspections + To 5 Tins fora FDA Inseaction + {Computer Syslom Validation in Pharmaceuticals + Why Pair lanes invested During incubation? + Prncile of UV Specvoghotametar + Maintenance of Pharmaceutical Clean Area: FDA Recommendation Diferent Storage Condions in Pharmaceuticals + Qualy Risk Manaas istorii Cleanroom tin Pharmaceuticals sesh+ Importance of Mixing Time n Blend Uniformity + Technology Transfor Guidelines for Pharmaceuticals “+ Hold Time Study in Pharmaceutical Manufacturing + Preparation for GMP Aust in Pharmaceuticals + Made of Action of Disinfectant Solutions + Dotergents Used for Cleaning of Pharmaceutical Equipments + Preoaratio of Balch Manufacturing Record (BMR) «+ Blsk of TSE and BSE in Pharmaccutioal Products + Pharmaceutical Contamination Conta! + Microbial Resistance agains! Disinfectants Used for Cleaning + Why Tool for Roo! Cause Analysis in Pharmacoutcale DifarentTyaes of Stainless Stee! for Pharmaceuticals ‘EDA’ Data Ileony Issues in Indian Facies [NOEL and MACO Calculations in Cleaning Validation Media Fil Test Failure Investgaton ‘dentiicaton of Envrormental isolates ‘Equipment Lubricants Used in Pharmacoutcals + 2.Sigma Formula for Trend Analy ims + EDA Fos Generally Used in Pharmaceutical Inspection DA Form 489 and Warning Letters ‘She Life Estimation of Pharmaceutical Products + Samalig and Testing in Exhibit and Process Validation Batches Planning ang Procedure flowed During Regulatory Audis + Revalidation of Pharmaceutea Pr ‘Audit Tall Requirements in Pharmaceuticals [Layout for Injection Manufacturing Unt ‘Sampling Plan SORT nt (ine for Phamacoutcals A ass boxes in Claes + Valiation of Pure Steam ‘Dead Leg and ts Lit in Water Systems Annual Product Qualty Review (APORJAPR/POR) in Quality Improvements "Wy 70% Isopropyl Alcohl (PA) is used as Disinfectant in Pharmaceuticals? (Checklist for Austin Laundry ‘Soparato Manufacturing Facily is Required for Manufacturing of Penicilin and Non peniclin Products + Whats Change Contral? + Prevention of Cross: contamination by HVAG in Pharmaceuticals CGMP Ault Check List- Personnel ang Premises (GMP Aut Check List: Water Supoly System + GMP Aucit Check List Weighing and Dispensing + GMP Aucit Check List. Storage of Staring Matorals + Cutent Gaod Manufacluing Practices - cGMP in Pharmaceutical Industies + Process Validation io Pharmaceutical Manufacturing + Conectve Action and Preventive Action (CAPA) + SOP for Corrective Acton and Preventve Action (CAPA) + Cleaning and Houseke + What does WHO + GMP Aucit Check List Filing and Packaging + GMP Ault Chock List Santaton and Hygione on tn arenapietn or ping Procedure in Pharme bout cross-conter scale