Pharmaceutical News & Regulatory Info

Mitigating Risks and Reducing Timelines in CMC for ATMPs & CGTs

Mitigating Risks and Reducing Timelines in CMC for ATMPs & CGTs

Shilpam Rajput2025-04-10T12:34:03+00:00April 10th, 2025|

IDMP Compliance for Pharma: Strategy & Benefits

IDMP Compliance for Pharma: Strategy & Benefits

Shilpam Rajput2025-04-08T07:49:53+00:00April 8th, 2025|

Key Takeaways From RSIDM Regulatory Forum 2025

Key Takeaways From RSIDM Regulatory Forum 2025

Shilpam Rajput2025-03-31T12:37:19+00:00March 31st, 2025|

Navigating Regulatory Challenges for Generic Inhalation Drug Products: A Strategic Approach

Navigating Regulatory Challenges for Generic Inhalation Drug Products: A Strategic Approach

Shilpam Rajput2025-03-27T10:25:46+00:00March 27th, 2025|

Navigating the Complex CMC Landscape of ATMPs and CGTs

Navigating the Complex CMC Landscape of ATMPs and CGTs

Shilpam Rajput2025-04-10T12:31:32+00:00March 17th, 2025|

ATMP Regulation in the EU and US: Global Convergence?

ATMP Regulation in the EU and US: Global Convergence?

Shilpam Rajput2025-04-10T12:30:01+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|

Pharmaceuticals Blog

Mitigating Risks and Reducing Timelines in CMC for ATMPs & CGTs

Mitigating Risks and Reducing Timelines in CMC for ATMPs & CGTs

IDMP Compliance for Pharma: Strategy & Benefits

IDMP Compliance for Pharma: Strategy & Benefits

Key Takeaways From RSIDM Regulatory Forum 2025

Key Takeaways From RSIDM Regulatory Forum 2025

Navigating Regulatory Challenges for Generic Inhalation Drug Products: A Strategic Approach

Navigating Regulatory Challenges for Generic Inhalation Drug Products: A Strategic Approach

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

Pharma Resources

Meet Dossplorer

Complimentary Consultation with a Celegence Expert

Our Pharma Services