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dissolution test guidelines

Analytical Method Development, Pharmaceutical R&D

Dissolution Test Guidelines by USP and EMA: A Regulatory Perspective

By Mohamed Fathy / October 15, 2025 / 17 minutes of reading

Dissolution Test Guidelines by USP and EMA: A Regulatory Perspective Read Post »

CTD module 1:admiistrative and regional information

Regulatory Affairs, PharmaCoresGeneralTopics

CTD Module 1: Administrative and Regional Information – The Foundation of Regulatory Submissions

By Naila Kanwal / October 13, 2025 / 9 minutes of reading

CTD Module 1: Administrative and Regional Information – The Foundation of Regulatory Submissions Read Post »

remove pharmacores and remove CTD series by pharmacores - small the size of the unified format transforming global drug approvals

Regulatory Affairs

CTD Demystified: Simplifying Global Approvals and Eliminating Compliance Barriers

By Naila Kanwal / October 10, 2025 / 7 minutes of reading

CTD Demystified: Simplifying Global Approvals and Eliminating Compliance Barriers Read Post »

pharmacovigilance and Ai in 2025

Pharmacovigilance, Uncategorized

Pharmacovigilance and Artificial Intelligence: Where We Stand in 2025

By Humraaz Kaja / October 3, 2025 / 7 minutes of reading

Pharmacovigilance and Artificial Intelligence: Where We Stand in 2025 Read Post »

Quantum-Enhanced Drug Formulation

Pharmaceutical R&D, Formulation Development

Quantum-Enhanced Drug Formulation: Perfect Designs From Months to 15 Minutes. (Part 01)

By Shaima Rana / September 26, 2025 / 14 minutes of reading

Quantum-Enhanced Drug Formulation: Perfect Designs From Months to 15 Minutes. (Part 01) Read Post »

Melt Granulation

Formulation Development

Melt Granulation: 5 Deep Dive Fruitful points into the alchemy of agglomeration

By Hanady Naeem / September 26, 2025 / 7 minutes of reading

Melt Granulation: 5 Deep Dive Fruitful points into the alchemy of agglomeration Read Post »

Pharmaceutical R&D, Analytical Method Development

Dissolution Test: How to Interpret Profiles and Understand Similarity Factor

By Mohamed Fathy / September 12, 2025 / 20 minutes of reading

Dissolution Test: How to Interpret Profiles and Understand Similarity Factor Read Post »

MRP

Production, Production Scheduling

Production & Material Requirement Planning (MRP): Key Areas, Processes & Best Practices

By Mirza Yasir / September 12, 2025 / 8 minutes of reading

Production & Material Requirement Planning (MRP): Key Areas, Processes & Best Practices Read Post »

IND ethics

Regulatory Affairs

What Are IND Ethics & Safety Requirements? FDA Clinical Trial Guide

By Naila Kanwal / September 11, 2025 / 8 minutes of reading

What Are IND Ethics & Safety Requirements? FDA Clinical Trial Guide Read Post »

Dry Granulation Process Overview

Pharmaceutical R&D, Formulation Development

Why Choose Dry Granulation? Slugging vs. Roller Compaction, Binders, and Industry Applications

By PharmaCores Scientific Team / September 8, 2025 / 8 minutes of reading

Why Choose Dry Granulation? Slugging vs. Roller Compaction, Binders, and Industry Applications Read Post »

how to obtain IND approval

Regulatory Affairs

IND (Investigational New Drug): 6 Critical and game- changing steps That Makes or Break Clinical Trial Approval

By Naila Kanwal / September 4, 2025 / 15 minutes of reading

IND (Investigational New Drug): 6 Critical and game- changing steps That Makes or Break Clinical Trial Approval Read Post »

Analytical Method Development, Pharmaceutical R&D

Dissolution Test Method Development: Ultimate practical guide (Part 2)

By Mohamed Fathy / August 29, 2025 / 8 minutes of reading

Dissolution Test Method Development: Ultimate practical guide (Part 2) Read Post »

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