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Posts by category

• Category: Analysis
  • Analysis of Azithromycin Tablet 500
• Category: Audit
  • SOP for Vendor Audit (Supplier Audit)
  • How to Handle Audits in Pharmaceuticals
  • SOP for Internal Audit
• Category: Calibration
  • SOP for Calibration of Autoclave by Indicators
  • Calibration in the Pharmaceutical Industry
• Category: CAPA
  • Effective CAPA (Corrective and Preventive Action)
• Category: Cleaning
• Category: Drugs
• Category: Education
  • Top 10 Best Private University for Pharmacy in Bangladesh
  • Biopharmaceutics Classification System (BCS)
  • Propylene Glycol vs Ethylene Glycol: Differences
  • Propylene Glycol in Pharmaceuticals
  • The Role of Pharmacists in Patient Management
  • Zinc Shampoo for Itching Scalp and Hair Loss
  • Computer-Aided Drug Design (CADD) in Pharma
  • Difference Between Drugs and Medicines
  • IQ OQ PQ in the Pharmaceuticals
  • Precision Medicine/Personalized Medicine
  • Best New 100 Questions and Answers About Pharmaceutical
• Category: Engg. SOPs
  • SOP for Preventive Maintenance of DM Plant
  • SOP for Leak Test of HEPA Filters
  • SOP for Guidelines for Maintenance Procedures
  • SOP for Planned Preventive Maintenance Schedule (PPM)
• Category: GMP
  • WHO GMP Guideline Complete for Pharmaceutical Industry (2026)
  • 10 Golden Rules of GMP
  • Best GMP Training Program and Schedule 2025
  • Best GMP Cleaning and Sanitation in Pharmaceuticals
  • Best GMP Guidelines for Pharmaceutical Industry
• Category: GMP Training
• Category: Guidelines
  • Good Regulatory Practices (GRP) in Pharmaceuticals: WHO Guidelines & Importance
  • 7 Quality Management Principles for ISO 9001:2015
  • Effective Good Cold Chain Management Practices in Pharmaceuticals
  • Drug Master File (DMF) Submission Guidelines FDA
  • Pharmaceutical Dossier Prepare & Submission Process 2025: A Step-by-Step Guide
  • Best Authorization Contact Committee (CCR)
  • Good Clinical Practice (GCP)
  • What are Guidelines for DGDA
  • FIFO, LIFO, FEFO Methods in Inventory Control
• Category: GxP
  • GxP in The Pharmaceuticals Industry
• Category: Health News
  • (Heart) Cardiac Stent Price in Bangladesh 2026: Latest Price
  • Ad-din Medical College Hospital Moghbazar:  Affordable Healthcare Excellence in Bangladesh
  • Measles Outbreak in Bangladesh 2026: Causes, Symptoms, and the Future of Immunization
  • Dengue Fever Outbreak in Bangladesh 2025
  • World Pharmacists Day 2025: Think Health, Think Pharmacist
  • Bangavax Vaccine: Bangladesh’s First mRNA COVID-19 Vaccine Receives US Patent Approval
  • Best Practice for Rational Use of Drugs
  • Los Angeles Wildfires and Health Impact on the Community
  • Human Metapneumovirus (HMPV) Symptoms & Treatment
  • China Calls HMPV Outbreak ‘Winter Occurrence’, India Says ‘Don’t Panic’
• Category: Interview Questions
  • New Interview Questions and Answers for PPIC 2024
• Category: ISO
• Category: Microbiology
  • Effective (NVPM) Non-Viable Particle Monitoring in Pharmaceutical Cleanrooms
  • Essential Microbiological Testing in Pharmaceuticals
  • Bacterial Endotoxin Test Procedure for Pharma
  • Sterility Testing Method in Pharmaceuticals
  • Bioburden Testing in Pharmaceuticals
  • Biological Indicator for Steam Sterilization
  • Pharmaceutical Microbiology
• Category: Microbiology SOPs
  • SOP for Settle Plates of Environmental Monitoring
  • SOP for Qualification of Autoclave
  • SOP for Growth Promotion Test of Media
  • SOP for Maintenance of Stock Cultures in Microbiology
• Category: PD SOPs
  • SOP for Stability Testing in Pharmaceutical
  • SOP for Product Development Planning
• Category: Pharma Education
  • Sieve Number vs Mesh Number: What’s the Difference?
• Category: Pharma Information
  • Top 30 Pharmaceutical Companies in Bangladesh 2026
  • Bangladesh Pharmaceutical Market Growth Forecast (2026–2030)
  • Novartis Bangladesh Changes Name to Nevian Lifescience PLC
  • Russia’s Cancer Vaccine Enteromix Shows 100% Success in Early Trials
  • Top Pharmaceutical Jobs in Bangladesh: Career & Salary
  • Bangladesh Pharmaceutical Export Market 2025 & Future Outlook
  • The Pharmaceutical Industry: A Pillar of Global Health and Innovation 2025
  • Types of Agreement in the Pharmaceutical Industry
  • Contract Manufacturing in Pharma: Best Technique
  • Beloved World Pharmacists Day 2024
  • Best Global Top 20 Pharmaceutical Companies in 2024
  • List of Pharmaceutical Company in Bangladesh 2024
• Category: Pharma Jobs
• Category: Pharma SOPs
  • SOP For Cleaning of Manufacturing Equipment
  • SOP for Antimicrobial Effectiveness Test: EP/USP
  • SOP for Cleaning and Sanitation of Warehouse Area
  • Batch Numbering SOP for Finished Products
  • SOP for Cleaning of QC Laboratory
  • SOP for Training and Evaluation of the Employee
  • SOP for Annual Product Quality Reviews (APQR)
  • SOP for Batch Numbering System of Raw and Packaging Materials.
  • SOP in the Pharmaceutical industry
• Category: Pharma Technology
  • RABS vs. Isolators
• Category: Pharmaceutical Trends
  • SUBA® Itraconazole Bioavailability Technology
• Category: Pharmacovigilance
  • Good Pharmacovigilance Practices (GVP)
  • SOP for Pharmacovigilance Surveillance Procedure
  • What is Pharmacovigilance?
• Category: PMD
  • Pharmaceutical Marketing System and Global Share
  • Supply Chain Management (SCM) in the Pharmaceuticals
  • Product Management Department in The Pharmaceutical Industry (PMD)
• Category: PPIC
  • Role of PPIC in Pharmaceuticals (Production Planning & Inventory Control)
• Category: Private University
  • Private & Public University for Pharmacy in Bangladesh: PCB list 2025
• Category: Product Development
  • Benzoic Acid and Salicylic Acid Ointment Process
  • SOP for Formulation Development in Pharmaceutical
  • Cefixime Trihydrate PFS Formulation and Manufacturing Process 2024
  • Azithromycin PFS Formulation and Manufacturing Process
  • Stability Study Protocol Template of Tablet
• Category: Production
  • Advanced Isolators Technologies in Modern Pharmaceutical Manufacturing
  • RABS-(Restricted Access Barrier Systems)
  • Isolator and Critical Cleanrooms
  • Principles and Applications of Fluid Bed Dryer (FBD)
  • Tablet Manufacturing Process in Pharma
  • Common Tablet Defects and Remedies in Manufacturing
  • DNS IV Infusion Post-Manufacturing Cloudiness Problem
• Category: Production SOPs
  • SOP for Operating Procedure of Multi Mill Machine
  • SOP For Cleaning Procedure of Production Area
• Category: QA SOPs
  • Best SOP for Dossier Preparation in Pharmaceuticals
  • Effective SOP for Quality Records Disposal
  • SOP for Change Control Procedure
  • SOP for Qualifications Protocol (IQ, OQ & PQ)
  • SOP for Corrective and Preventive Actions (CAPA)
  • SOP for Handling Deviations
  • SOP for Environment Monitoring Procedure
  • SOP for Basic GMP Requirements in Production Area
  • SOP for Training Records
  • SOP of SOP in Pharmaceutical Industry
• Category: QC SOPs
  • SOP for Out of Specification (OOS)
  • SOP for Karl Fischer Operating Procedure
  • SOP for Operation of FTIR Spectrometer
  • SOP for Operation of Dissolution Test Apparatus
  • SOP for Good Laboratory Practices (GLP)
  • SOP for Operating Procedure of HPLC
  • SOP for Operation of UV-Vis Spectrophotometer
  • SOP for Calibration of Karl Fischer Apparatus
  • SOP for HPLC Column Cleaning
  • SOP for Calibration of UV-Vis Spectrophotometer
  • SOP for Calibration of FTIR Apparatus
  • SOP for Calibration of HPLC
  • SOP for Calibration of Dissolution Test Apparatus
  • SOP for Disposal of Rejected Materials
  • SOP for Handling and Usage of Hazardous Chemicals
  • SOP for Sampling Method of Packaging Materials
  • SOP for Chemical Laboratory Safety
  • SOP For Sampling Method of Raw Materials
  • SOP for Cleaning of Sampling Tools
  • SOP for Storage and Use of CRS (Chemical Reference Standard)
  • SOP for Qualification of Working Standard
  • New SOP for Operating of Steam Sterilizer
• Category: Qualification
  • (IQ, OQ & PQ) Qualifications of Injectable Tank
• Category: Quality Assurance
  • Effective Cleaning Validation SOP in Pharmaceutical Industry
  • Quality Management System (QMS) in Pharmaceuticals
  • Best CAPA Verification Process in Pharmaceuticals
  • Checklist for Reviewing BMR, BCR and BPR in Pharma
  • CAPA (Corrective and Preventive Action) in Pharmaceuticals
  • APQR Annual Product Quality Review
• Category: Quality Control
  • Root Cause Analysis (RCA) in Pharmaceuticals
  • HPLC Column Cleaning Solution in Pharmaceuticals
  • Prepare and Standardize 0.5 N Hydrochloric Acid
  • Prepare and Standardize 0.1 N Hydrochloric Acid VS
  • Prepare and Standardize 1 N Hydrochloric Acid VS
  • Prepare and Standardize 1 N Sodium Hydroxide VS
  • Prepare and Standardize 0.1 N Sodium Hydroxide VS
  • Prepare and Standardize 0.5 N Sodium Hydroxide VS
  • Difference Between Water and Moisture Content
• Category: Regulatory
  • How to Register a New Pharmaceutical Company
  • Common Technical Document (CTD) Modules
• Category: Regulatory Affairs
• Category: Regulatory Guidelines
• Category: Testing Procedure
  • Beta-lactam Test for Personnel in Manufacturing
• Category: Top 10
  • Top 30 Pharmaceutical Company in Bangladesh 2025 : IQVIA QTR 2Q 2025 Data
  • Top 50 Pharmaceutical Company in Bangladesh 2025
  • Top 10 Best University in Bangladesh for Pharmacy 2025
  • Top 10 Pharmaceutical Companies in India 2025
  • Top 20 Best-selling Drugs Globally in 2025
  • Top 20 Pharmaceutical Company in Bangladesh 2024
  • Top 10 Pharmaceutical Companies in USA 2024
• Category: Top 30
• Category: Top Pharma Company
• Category: Validation
  • Process Validation vs. Product Validation in Pharmaceuticals
  • Best Revalidation Activities in Pharmaceuticals
  • Types of Pharmaceutical Contaminants
  • MACO (Maximum Allowable Carryover) Calculation
  • Cleaning Validation Report of Microbiology Lab
  • Cleaning Validation Protocol for Microbiology lab
  • Cleaning Validation Protocol for Quality Control
  • Cleaning Validation Protocol for Production Area in Pharmaceuticals
  • Cleaning Validation Master Plan (CVMP)
  • Pharmaceutical Validation Program
  • What is Validation Report
  • Validation Schedule in Pharmaceuticals
  • New Best Validation Protocol Writing Techniques 2023
  • SOP for Concurrent Process Validation
• Category: Warehouse
• Category: Warehouse SOPs
  • Best SOP for Environmental Monitoring in Warehouse
  • SOP for Temperature and Relative Humidity Record
  • Best SOP for Pest Control in Warehouse
  • Effective SOP for Good Warehousing Practices (GWP)
  • SOP for Warehouse Operations Overview
  • SOP for Receiving of Raw and Packaging Materials
  • SOP for Labeling of Raw and Packaging Materials
  • SOP for Dress Changing Procedure of Personnel in Warehouse
• Category: WHO
  • WHO Technical Report Series (TRS) and Annexes

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