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Author name: Naila Kanwal

IND

PharmaCoresGeneralTopics, 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 »

Pharmaceutical regulation bodies

Regulatory Affairs

Global Health Regulation: 3 Key Power Struggles Between FDA, EMA, WHO & Others

By Naila Kanwal / August 13, 2025 / 11 minutes of reading

Global Health Regulation: 3 Key Power Struggles Between FDA, EMA, WHO & Others Read Post »

Regulatory Affairs

Regulatory Affairs Career Breakthrough: Expert Interview Strategies & Success Tips for 2025

By Naila Kanwal / August 9, 2025 / 8 minutes of reading

Regulatory Affairs Career Breakthrough: Expert Interview Strategies & Success Tips for 2025 Read Post »

"From R&D to Market: Regulatory Milestones in Drug Development Lifecycle

Regulatory Affairs

Strategic Regulatory Milestones in Drug Development Lifecycle : Unlocking Market Success from R&D

By Naila Kanwal / July 22, 2025 / 9 minutes of reading

Strategic Regulatory Milestones in Drug Development Lifecycle : Unlocking Market Success from R&D Read Post »

Drug Dissolution Equipment Illustration

Analytical Method Development, Pharmaceutical R&D

Drug Dissolution: A Beginner’s Guide to Testing, Apparatus, and Release Profiles

By Naila Kanwal / June 30, 2025 / 7 minutes of reading

Drug Dissolution: A Beginner’s Guide to Testing, Apparatus, and Release Profiles Read Post »

pharmaceutical regulatory affairs

Regulatory Affairs

Comprehensive Guide to Pharmaceutical Regulatory Affairs: Key Functions, Scope, and Industry Importance.

By Naila Kanwal / June 24, 2025 / 9 minutes of reading

Comprehensive Guide to Pharmaceutical Regulatory Affairs: Key Functions, Scope, and Industry Importance. Read Post »

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