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.

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

Celegence2023-10-26T10:31:50+00:00

Regulatory Affairs Support Pharmaceutical Case Study - Feature

Regulatory affairs support, Publishing & Submissions and Solutions for a young pharmaceutical company

Celegence2024-04-24T15:30:48+00:00

Biopharmaceutical Company San Francisco - Nonclinical Data Processing - Celegence - Feature

Centre of Excellence Model to Streamline Nonclinical Data Processing and Presentation in Contributor Reports

Celegence2023-05-31T15:14:38+00:00

ECTD Publishing for Global Healthcare Company - Case Study - Feature

ECTD Publishing (Global) for Global Healthcare Company

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Webinars

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

Medical Device Virtual Summit – Afternoon Program

Medical Device Virtual Summit – Afternoon Program

Celegence2024-02-14T06:21:53+00:00April 28th, 2021|

Medical Device Virtual Summit – Morning Program

Medical Device Virtual Summit – Morning Program

Celegence2024-02-14T06:21:25+00:00April 28th, 2021|

Clinical Evaluations for Unique Product Types Under the EU MDR – Webinar

Clinical Evaluations for Unique Product Types Under the EU MDR – Webinar

Celegence Admin2021-02-09T16:29:05+00:00October 19th, 2020|

How to Start Preparing Your Team for the EUDAMED Database – Webinar

How to Start Preparing Your Team for the EUDAMED Database – Webinar

Celegence2021-02-09T16:29:07+00:00August 31st, 2020|

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News

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

Navigating the MDR/IVDR Conformity Assessment Maze: Pitfalls and Pathways

Navigating the MDR/IVDR Conformity Assessment Maze: Pitfalls and Pathways

Celegence2024-04-29T15:39:15+00:00April 29th, 2024|

Strategies for Successful Post-Market Clinical Follow-Up (PMCF) under EU MDR: Insights from a Comprehensive Webinar

Strategies for Successful Post-Market Clinical Follow-Up (PMCF) under EU MDR: Insights from a Comprehensive Webinar

Shilpam Rajput2024-04-22T17:18:59+00:00April 19th, 2024|

RAPS Euro Convergence 2024

RAPS Euro Convergence 2024

Celegence2024-04-25T15:02:02+00:00April 18th, 2024|

AI-Powered Solutions for Regulatory Compliance in the Medical Device Industry

AI-Powered Solutions for Regulatory Compliance in the Medical Device Industry

Celegence2024-04-11T11:07:45+00:00April 5th, 2024|

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Pharmaceuticals

Case Studies

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

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

Regulatory affairs support, Publishing & Submissions and Solutions for a young pharmaceutical company

Regulatory affairs support, Publishing & Submissions and Solutions for a young pharmaceutical company

Centre of Excellence Model to Streamline Nonclinical Data Processing and Presentation in Contributor Reports

Centre of Excellence Model to Streamline Nonclinical Data Processing and Presentation in Contributor Reports

ECTD Publishing (Global) for Global Healthcare Company

ECTD Publishing (Global) for Global Healthcare Company

Webinars

Medical Device Virtual Summit – Afternoon Program

Medical Device Virtual Summit – Afternoon Program

Medical Device Virtual Summit – Morning Program

Medical Device Virtual Summit – Morning Program

Clinical Evaluations for Unique Product Types Under the EU MDR – Webinar

Clinical Evaluations for Unique Product Types Under the EU MDR – Webinar

How to Start Preparing Your Team for the EUDAMED Database – Webinar

How to Start Preparing Your Team for the EUDAMED Database – Webinar

News

Navigating the MDR/IVDR Conformity Assessment Maze: Pitfalls and Pathways

Navigating the MDR/IVDR Conformity Assessment Maze: Pitfalls and Pathways

Strategies for Successful Post-Market Clinical Follow-Up (PMCF) under EU MDR: Insights from a Comprehensive Webinar

Strategies for Successful Post-Market Clinical Follow-Up (PMCF) under EU MDR: Insights from a Comprehensive Webinar

RAPS Euro Convergence 2024

RAPS Euro Convergence 2024

AI-Powered Solutions for Regulatory Compliance in the Medical Device Industry

AI-Powered Solutions for Regulatory Compliance in the Medical Device Industry

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