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Author name: naila_kanwal

CTD Module 1.3 Labeling & Product Info for Patient Safety

Regulatory Affairs, Uncategorized

CTD Module 1.3 Labeling and Product information: Ensuring Patient Safety or Risking Miscommunication

By naila_kanwal / November 9, 2025 / 7 minutes of reading

CTD Module 1.3 Labeling and Product information: Ensuring Patient Safety or Risking Miscommunication 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 »

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 »

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 »

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 »

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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