Case Study: Regulatory and Market Intelligence Support for a Top-Tier Biotechnology Firm
Regulatory affairs support, Publishing & Submissions and Solutions for a young pharmaceutical company
Celegence2023-10-26T10:31:50+00:00Case Study: 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
Celegence2023-06-28T11:06:31+00:00Case Study: Centre of Excellence Model to Streamline Nonclinical Data Processing and Presentation in Contributor Reports
ECTD Publishing (Global) for Global Healthcare Company
Celegence2023-05-31T15:14:38+00:00Case Study: ECTD Publishing (Global) for Global Healthcare Company Project Summary:
RIMS & Compliance Data Management
Celegence2023-07-06T12:05:53+00:00Case Study: RIMS & Compliance Data Management Project Summary: A
RIMS & xEVMPD for Global Pharmaceutical Company
Celegence2023-05-18T05:22:28+00:00Case Study: RIMS & xEVMPD for Global Pharmaceutical Company Project Summary:
IDMP Data Governance for Global Regulatory Affairs, Production & Supply
Celegence2023-05-03T16:16:37+00:00Case Study: IDMP Data Governance for Global Regulatory Affairs, Production & Supply
Medical Writing for a Global Pharmaceutical Company
Celegence2023-05-03T14:50:25+00:00Case Study: Medical Writing for a Global Pharmaceutical Company Background –
CMC Authoring for a Global Healthcare Company
Celegence2023-01-16T18:57:23+00:00Case Study: CMC Authoring for a Global Healthcare Company Background –
Publishing Center of Excellence in the EU, US, Japan & China for a Global Pharmaceutical Company
Celegence2023-06-02T06:09:31+00:00Case Study: Publishing Center of Excellence in the European Union, United States, Japan, and China for
RIMS Business Process Training for a Global Pharmaceutical Company
Celegence2021-11-09T16:10:39+00:00Case Study: RIMS Business Process Training for a Global Pharmaceutical Company
EU MDR Template Creation for a Global Multinational Life Sciences Manufacturer
Celegence Admin2021-09-08T17:54:15+00:00Case Study: EU MDR Template Creation for a Global Multinational Life Sciences Manufacturer