Celegence Acquires Qdossier to Bolster its Regulatory Consultancy Services Celegence Acquires Qdossier to Bolster its Regulatory Consultancy ServicesCelegence Admin2022-08-04T15:40:22+00:00July 18th, 2022|
Report Writing Functionality added to EU MDR and IVDR Compliance Technology, CAPTIS™ Report Writing Functionality added to EU MDR and IVDR Compliance Technology, CAPTIS™Celegence Admin2022-07-20T20:25:16+00:00July 7th, 2022|
DIA 2022 Global Annual Meeting June 20-22 DIA 2022 Global Annual Meeting June 20-22Celegence Admin2022-06-06T14:57:51+00:00June 6th, 2022|
Building a Flexible and Future-Proof IDMP Data & Process Management Strategy Webinar Series Building a Flexible and Future-Proof IDMP Data & Process Management Strategy Webinar SeriesCelegence2022-08-04T15:39:13+00:00May 24th, 2022|
RAPS Euro Regulatory Convergence Conference 2022 RAPS Euro Regulatory Convergence Conference 2022Celegence2022-04-26T15:52:11+00:00April 26th, 2022|
Navigating eCTD Submissions in China – Webinar with James Ma – Q&A Navigating eCTD Submissions in China – Webinar with James Ma – Q&ACelegence Admin2022-03-22T15:46:47+00:00March 22nd, 2022|
Navigating eCTD Submissions in China – Webinar with James Ma – Transcript Navigating eCTD Submissions in China – Webinar with James Ma – TranscriptCelegence Admin2022-10-17T14:31:17+00:00March 16th, 2022|
Beyond Compliance: Preparing for IDMP Now and Into the Future Beyond Compliance: Preparing for IDMP Now and Into the FutureCelegence2022-08-04T15:39:33+00:00November 16th, 2021|
Navigating eCTD Submissions in China – Webinar Navigating eCTD Submissions in China – WebinarCelegence2021-08-10T15:23:54+00:00August 10th, 2021|
Regulatory Medical Writing: The Hurdles of Authoring Company Core Data Sheet (CCDS) Documents Regulatory Medical Writing: The Hurdles of Authoring Company Core Data Sheet (CCDS) DocumentsCelegence2021-05-11T10:21:50+00:00May 6th, 2021|