Pharmaceuticals

Explore our library of pharmaceutical industry news articles, webinars, insights, and case studies.

Case Studies

Learn how Celegence has successfully assisted pharma organizations around the world to navigate critical regulatory challenges and more.

Shilpam Rajput2024-10-15T05:29:50+00:00

Implementation of Veeva Vault IDMP Functionality for a Global Pharmaceutical Company

Shilpam Rajput2024-10-04T10:22:39+00:00

IDMP Data Migration & Integration for a Global Pharmaceutical Company

Shilpam Rajput2024-09-13T12:33:46+00:00

IDMP Data Analysis & Remediation for a Global Pharmaceutical Company

Celegence2023-08-15T12:12:33+00:00

Regulatory Market Intelligence Support Top Biotechnology Firm - Case Study - Feature

Regulatory and Market Intelligence Support for a Top-Tier Biotechnology Firm

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Webinars

Learn about upcoming Celegence pharmaceutical webinars, and access previous broadcasts.

Unlock the Future of Regulatory Submissions: Join Our Lean Authoring Webinar

Unlock the Future of Regulatory Submissions: Join Our Lean Authoring Webinar

Shilpam Rajput2024-11-15T05:23:37+00:00October 22nd, 2024|

Discussing Regulatory Affairs Leadership Perspectives – 2024 Survey Insights

Discussing Regulatory Affairs Leadership Perspectives – 2024 Survey Insights

Shilpam Rajput2024-09-18T14:34:05+00:00June 26th, 2024|

Webinar – EU Pharmaceutical Reform: Unveiling Draft Legislation Impacts

Webinar – EU Pharmaceutical Reform: Unveiling Draft Legislation Impacts

Celegence2024-09-18T14:34:14+00:00February 2nd, 2024|

Practical Advice and Next Steps to Ensure PLM Portal Readiness Webinar

Practical Advice and Next Steps to Ensure PLM Portal Readiness Webinar

Celegence2024-01-23T15:16:06+00:00January 23rd, 2024|

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News

The latest news and insights of the pharmaceutical industry from our expert global team.

Navigate EU Scientific Advice with Confidence – Whitepaper

Navigate EU Scientific Advice with Confidence – Whitepaper

Shilpam Rajput2024-11-19T14:31:33+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|

Ad/Promo Submissions to the FDA: Process, Transition, and Compliance with eCTD

Ad/Promo Submissions to the FDA: Process, Transition, and Compliance with eCTD

Celegence2024-11-12T12:37:04+00:00November 12th, 2024|

Streamlining IDMP Compliance with Effective Master Data Management

Streamlining IDMP Compliance with Effective Master Data Management

Celegence2024-10-31T15:55:48+00:00October 31st, 2024|

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Pharmaceuticals

Case Studies

Implementation of Veeva Vault IDMP Functionality for a Global Pharmaceutical Company

Implementation of Veeva Vault IDMP Functionality for a Global Pharmaceutical Company

IDMP Data Migration & Integration for a Global Pharmaceutical Company

IDMP Data Migration & Integration for a Global Pharmaceutical Company

IDMP Data Analysis & Remediation for a Global Pharmaceutical Company

IDMP Data Analysis & Remediation for a Global Pharmaceutical Company

Regulatory and Market Intelligence Support for a Top-Tier Biotechnology Firm

Regulatory and Market Intelligence Support for a Top-Tier Biotechnology Firm

Webinars

Unlock the Future of Regulatory Submissions: Join Our Lean Authoring Webinar

Unlock the Future of Regulatory Submissions: Join Our Lean Authoring Webinar

Discussing Regulatory Affairs Leadership Perspectives – 2024 Survey Insights

Discussing Regulatory Affairs Leadership Perspectives – 2024 Survey Insights

Webinar – EU Pharmaceutical Reform: Unveiling Draft Legislation Impacts

Webinar – EU Pharmaceutical Reform: Unveiling Draft Legislation Impacts

Practical Advice and Next Steps to Ensure PLM Portal Readiness Webinar

Practical Advice and Next Steps to Ensure PLM Portal Readiness Webinar

News

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

Ad/Promo Submissions to the FDA: Process, Transition, and Compliance with eCTD

Ad/Promo Submissions to the FDA: Process, Transition, and Compliance with eCTD

Streamlining IDMP Compliance with Effective Master Data Management

Streamlining IDMP Compliance with Effective Master Data Management

Pharma Resources

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