Pharmaceutical News & Regulatory Info

Navigating the Complex CMC Landscape of ATMPs and CGTs

Navigating the Complex CMC Landscape of ATMPs and CGTs

Shilpam Rajput2025-03-17T06:13:52+00:00March 17th, 2025|

ATMP Regulation in the EU and US: Global Convergence?

ATMP Regulation in the EU and US: Global Convergence?

Shilpam Rajput2025-03-11T07:14:59+00:00March 11th, 2025|

Understanding the Critical Role of CMC Dossiers in Pharmaceutical Regulatory Submissions

Understanding the Critical Role of CMC Dossiers in Pharmaceutical Regulatory Submissions

Shilpam Rajput2025-02-25T05:18:57+00:00February 24th, 2025|

Unlocking the Potential of RPA in Regulatory Affairs: A Strategic Guide

Unlocking the Potential of RPA in Regulatory Affairs: A Strategic Guide

Shilpam Rajput2025-01-30T14:34:55+00:00January 29th, 2025|

Efficiency in Regulatory Submissions with Lean Authoring: Save Time, Improve Compliance, and Streamline Global Regulatory Documentation Processes

Efficiency in Regulatory Submissions with Lean Authoring: Save Time, Improve Compliance, and Streamline Global Regulatory Documentation Processes

Shilpam Rajput2025-01-22T15:30:41+00:00January 17th, 2025|

Exploring the Advantages of eCTD 4.0

Exploring the Advantages of eCTD 4.0

Celegence2025-02-12T15:59:59+00:00December 5th, 2024|

Pharmaceutical Focus Group Shares Best Practices in Regulatory Publishing and Submissions

Pharmaceutical Focus Group Shares Best Practices in Regulatory Publishing and Submissions

Celegence2024-11-28T12:48:11+00:00November 28th, 2024|

RAPS – Regulatory Readiness & Resources 2024

RAPS – Regulatory Readiness & Resources 2024

Shilpam Rajput2024-11-22T09:56:54+00:00November 22nd, 2024|

Navigate EU Scientific Advice with Confidence – Whitepaper

Navigate EU Scientific Advice with Confidence – Whitepaper

Shilpam Rajput2024-12-06T09:54:45+00:00November 19th, 2024|

Lean Authoring Checklist for Streamlined Regulatory Submissions

Lean Authoring Checklist for Streamlined Regulatory Submissions

Shilpam Rajput2024-11-19T07:14:28+00:00November 18th, 2024|

Pharmaceuticals Blog

Navigating the Complex CMC Landscape of ATMPs and CGTs

Navigating the Complex CMC Landscape of ATMPs and CGTs

ATMP Regulation in the EU and US: Global Convergence?

ATMP Regulation in the EU and US: Global Convergence?

Understanding the Critical Role of CMC Dossiers in Pharmaceutical Regulatory Submissions

Understanding the Critical Role of CMC Dossiers in Pharmaceutical Regulatory Submissions

Unlocking the Potential of RPA in Regulatory Affairs: A Strategic Guide

Unlocking the Potential of RPA in Regulatory Affairs: A Strategic Guide

Efficiency in Regulatory Submissions with Lean Authoring: Save Time, Improve Compliance, and Streamline Global Regulatory Documentation Processes

Efficiency in Regulatory Submissions with Lean Authoring: Save Time, Improve Compliance, and Streamline Global Regulatory Documentation Processes

Exploring the Advantages of eCTD 4.0

Exploring the Advantages of eCTD 4.0

Pharmaceutical Focus Group Shares Best Practices in Regulatory Publishing and Submissions

Pharmaceutical Focus Group Shares Best Practices in Regulatory Publishing and Submissions

RAPS – Regulatory Readiness & Resources 2024

RAPS – Regulatory Readiness & Resources 2024

Navigate EU Scientific Advice with Confidence – Whitepaper

Navigate EU Scientific Advice with Confidence – Whitepaper

Lean Authoring Checklist for Streamlined Regulatory Submissions

Lean Authoring Checklist for Streamlined Regulatory Submissions

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