Analytical Method Development, Pharmaceutical R&DMethod Development and QbD: 7 steps to Design Robust Analytical Methods with Science-Based Risk Assessment By Mohamed Fathy / 24-01-2026 / 11 minutes of reading Method Development and QbD: 7 steps to Design Robust Analytical Methods with Science-Based Risk Assessment Read Post ยป
PharmaCoresGeneralTopicsStability Studies of Pharmaceuticals: Ensuring Efficacy and Safety Over Time By Mohamed Fathy / 09-01-2026 / 9 minutes of reading Stability Studies of Pharmaceuticals: Ensuring Efficacy and Safety Over Time Read Post ยป
Advanced Drug Delivery Systems EngineeringThe Future Is Here: How 3D Printing Is Transforming Personalized Dosing By Mohamed Fathy / 04-01-2026 / 7 minutes of reading The Future Is Here: How 3D Printing Is Transforming Personalized Dosing Read Post ยป
Formulation DevelopmentElectrogenomic Formulations: Revolutionary Drug Delivery Systems That Respond to Cellular Gene Expression in Real Time (2026) (Part 01) By Mohamed Fathy / 28-12-2025 / 12 minutes of reading Electrogenomic Formulations: Revolutionary Drug Delivery Systems That Respond to Cellular Gene Expression in Real Time (2026) (Part 01) Read Post ยป
Operational Excellence in Pharmaceutical Industry, PharmaCoresGeneralTopics, Quality AssuranceOperational Excellence Episode 8: Building A Resilient Organization with Agility & Flexibility By Mohamed Fathy / 20-12-2025 / 12 minutes of reading Operational Excellence Episode 8: Building A Resilient Organization with Agility & Flexibility Read Post ยป
Regulatory AffairsWhat Are IND Ethics & Safety Requirements? FDA Clinical Trial Guide By Mohamed Fathy / 11-09-2025 / 8 minutes of reading What Are IND Ethics & Safety Requirements? FDA Clinical Trial Guide Read Post ยป
Formulation Development, Pharmaceutical R&DWhy Choose Dry Granulation? Slugging vs. Roller Compaction, Binders, and Industry Applications By Mohamed Fathy / 08-09-2025 / 8 minutes of reading Why Choose Dry Granulation? Slugging vs. Roller Compaction, Binders, and Industry Applications Read Post ยป
Regulatory AffairsIND (Investigational New Drug): 6 Critical and game- changing steps That Makes or Break Clinical Trial Approval By Mohamed Fathy / 04-09-2025 / 15 minutes of reading IND (Investigational New Drug): 6 Critical and game- changing steps That Makes or Break Clinical Trial Approval Read Post ยป
Analytical Method Development, Pharmaceutical R&DDissolution Test Method Development: Ultimate practical guide (Part 2) By Mohamed Fathy / 29-08-2025 / 8 minutes of reading Dissolution Test Method Development: Ultimate practical guide (Part 2) Read Post ยป
PharmaCoresGeneralTopicsPharmacoeconomics: Cost-Bene๏ฌt Analysis of Drugs By Mohamed Fathy / 29-08-2025 / 7 minutes of reading Pharmacoeconomics: Cost-Bene๏ฌt Analysis of Drugs Read Post ยป
Bioequivalence, Pharmaceutical R&DFrom Humans to Holograms: The Breakthrough Shift to Virtual Bioequivalence (vBE)&Goodbye Traditional BE Trials (Part 02) By Mohamed Fathy / 27-08-2025 / 21 minutes of reading From Humans to Holograms: The Breakthrough Shift to Virtual Bioequivalence (vBE)&Goodbye Traditional BE Trials (Part 02) Read Post ยป
Bioequivalence, Pharmaceutical R&DFrom Humans to Holograms: The Breakthrough Shift to Virtual Bioequivalence (vBE) & Goodbye Traditional BE Trials (Part 01) By Mohamed Fathy / 17-08-2025 / 12 minutes of reading From Humans to Holograms: The Breakthrough Shift to Virtual Bioequivalence (vBE) & Goodbye Traditional BE Trials (Part 01) Read Post ยป