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

Celegence2023-06-28T11:06:31+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

Celegence2023-07-06T12:05:53+00:00

RIMS & Compliance Data Management

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Webinars

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

Medical Device Virtual Summit – Morning Program

Medical Device Virtual Summit – Morning Program

Celegence2021-05-14T12:58:20+00:00April 28th, 2021|

Clinical Evaluations for Unique Product Types Under the EU MDR – Dr. Pratibha Mishra’s Presentation

Clinical Evaluations for Unique Product Types Under the EU MDR – Dr. Pratibha Mishra’s Presentation

Celegence Admin2022-10-17T14:21:34+00:00December 10th, 2020|

SaMD, Brexit & Market Surveillance – EUDAMED Database Webinar

SaMD, Brexit & Market Surveillance – EUDAMED Database Webinar

Celegence2022-10-17T14:25:13+00:00November 17th, 2020|

UDI & Product Types of Immediate Concern – EUDAMED Database Webinar

UDI & Product Types of Immediate Concern – EUDAMED Database Webinar

Celegence Admin2022-10-17T14:24:26+00:00November 10th, 2020|

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News

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

Systematic Literature Review Tools – What To Look For When Choosing One

Systematic Literature Review Tools – What To Look For When Choosing One

Celegence2023-09-13T11:40:03+00:00September 13th, 2023|

RAPS Regulatory Convergence 2023

RAPS Regulatory Convergence 2023

Celegence2023-09-05T17:03:42+00:00September 5th, 2023|

Optimizing CER and PMS Document Writing with Technology and AI – Webinar with Medtech Intelligence

Optimizing CER and PMS Document Writing with Technology and AI – Webinar with Medtech Intelligence

Celegence2023-08-30T13:41:06+00:00August 30th, 2023|

510k Submission Planning – Expert Tips for Medical Device Manufacturers

510k Submission Planning – Expert Tips for Medical Device Manufacturers

Celegence Admin2023-08-22T15:39:23+00:00August 22nd, 2023|

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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

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

RIMS & Compliance Data Management

RIMS & Compliance Data Management

Webinars

Medical Device Virtual Summit – Morning Program

Medical Device Virtual Summit – Morning Program

Clinical Evaluations for Unique Product Types Under the EU MDR – Dr. Pratibha Mishra’s Presentation

Clinical Evaluations for Unique Product Types Under the EU MDR – Dr. Pratibha Mishra’s Presentation

SaMD, Brexit & Market Surveillance – EUDAMED Database Webinar

SaMD, Brexit & Market Surveillance – EUDAMED Database Webinar

UDI & Product Types of Immediate Concern – EUDAMED Database Webinar

UDI & Product Types of Immediate Concern – EUDAMED Database Webinar

News

Systematic Literature Review Tools – What To Look For When Choosing One

Systematic Literature Review Tools – What To Look For When Choosing One

RAPS Regulatory Convergence 2023

RAPS Regulatory Convergence 2023

Optimizing CER and PMS Document Writing with Technology and AI – Webinar with Medtech Intelligence

Optimizing CER and PMS Document Writing with Technology and AI – Webinar with Medtech Intelligence

510k Submission Planning – Expert Tips for Medical Device Manufacturers

510k Submission Planning – Expert Tips for Medical Device Manufacturers

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