Celegence Expertise Interview: Joseph Richardson Larbi, Director and Medical Device SME
1:43
Celegence Expertise Interview: Joseph Richardson Larbi, Director and Medical Device SME
Ай бұрын
Celegence Expertise Interview: Insights from Lakshmeenarayana Goundalkar, Chief Delivery Officer
5:01
Celegence Expertise Interview: Insights from Lakshmeenarayana Goundalkar, Chief Delivery Officer
Ай бұрын
AI-Powered MDR Maintenance: The Future State of Regulatory Compliance
1:32
AI-Powered MDR Maintenance: The Future State of Regulatory Compliance
3 ай бұрын
Efficient collaboration in PMS document reviews - CAPTIS™ Software for EU MDR and IVDR Compliance
0:35
Efficient collaboration in PMS document reviews - CAPTIS™ Software for EU MDR and IVDR Compliance
10 ай бұрын
Standard Templates for PMS Documentation in CAPTIS™ - Software for EU MDR and IVDR Compliance
0:36
Standard Templates for PMS Documentation in CAPTIS™ - Software for EU MDR and IVDR Compliance
11 ай бұрын
Automated report writing with CAPTIS™ Data Dictionary - Software for EU MDR and IVDR Compliance
0:35
Automated report writing with CAPTIS™ Data Dictionary - Software for EU MDR and IVDR Compliance
11 ай бұрын
Is the EU MDR Extension a Blessing or a Curse? - Webinar
58:10
Is the EU MDR Extension a Blessing or a Curse? - Webinar
11 ай бұрын
CAPTIS™ Copilot - Most Advanced AI Compliance Solution for the Life Sciences Industry
0:31
CAPTIS™ Copilot - Most Advanced AI Compliance Solution for the Life Sciences Industry
11 ай бұрын
Automatic Content Linking in PMS Documentation with CAPTIS™ - Software for EU MDR & IVDR Compliance
0:36
Automatic Content Linking in PMS Documentation with CAPTIS™ - Software for EU MDR & IVDR Compliance
Жыл бұрын
CAPTIS™ - Software Solution for Dynamic Literature Tables
0:40
CAPTIS™ - Software Solution for Dynamic Literature Tables
Жыл бұрын
Easy Reference Management with CAPTIS™ - Software for EU MDR and IVDR Compliance
0:32
Easy Reference Management with CAPTIS™ - Software for EU MDR and IVDR Compliance
Жыл бұрын
Automated Abbreviation Management with CAPTIS™ - Software for EU MDR and IVDR Compliance
0:32
Automated Abbreviation Management with CAPTIS™ - Software for EU MDR and IVDR Compliance
Жыл бұрын
IVDR Survival Guide-Common Pitfalls Encountered in Complying with Regulation’s Requirements: Webinar
54:04
IVDR Survival Guide-Common Pitfalls Encountered in Complying with Regulation’s Requirements: Webinar
Жыл бұрын
Webinar - Clinical Evaluation of Dental Medical Devices - Lessons Learned from NB Assessments
59:04
Webinar - Clinical Evaluation of Dental Medical Devices - Lessons Learned from NB Assessments
Жыл бұрын
Dossplorer™ - Advanced Cloud-based Dossier Management Solution
2:11
Dossplorer™ - Advanced Cloud-based Dossier Management Solution
Жыл бұрын
Life Sciences Regulatory Solutions and Services - Overview of Celegence
2:46
Life Sciences Regulatory Solutions and Services - Overview of Celegence
Жыл бұрын
CAPTIS™ - Technology for EU MDR & IVDR Compliance
2:23
CAPTIS™ - Technology for EU MDR & IVDR Compliance
Жыл бұрын
Analysis of EU MDR & IVDR Amendment Proposal 2023/0005 - Celegence
13:52
Analysis of EU MDR & IVDR Amendment Proposal 2023/0005 - Celegence
Жыл бұрын
Implications for Medtech Companies with FDA Rollout of the New QMSR to Replace Current QSR - Webinar
43:43
Implications for Medtech Companies with FDA Rollout of the New QMSR to Replace Current QSR - Webinar
Жыл бұрын
Unlocking The Value Of Regulatory Dossiers With eCTD Viewing Technology - Dossplorer™ Webinar
38:42
Unlocking The Value Of Regulatory Dossiers With eCTD Viewing Technology - Dossplorer™ Webinar
Жыл бұрын
Navigating the In Vitro Diagnostic Regulation (IVDR) Rollout for Legacy & New Devices - Webinar
52:23
Navigating the In Vitro Diagnostic Regulation (IVDR) Rollout for Legacy & New Devices - Webinar
Жыл бұрын
Video Testimonial From Jim Talbot - Zap Surgical
1:45
Video Testimonial From Jim Talbot - Zap Surgical
Жыл бұрын
How to Optimize the ROI on Your RIMS Solution - Webinar
25:17
How to Optimize the ROI on Your RIMS Solution - Webinar
Жыл бұрын
Webinar - Process & Technology Innovation in EU MDR Compliance
40:58
Webinar - Process & Technology Innovation in EU MDR Compliance
Жыл бұрын
Navigating eCTD Submissions in China - Webinar
40:55
Navigating eCTD Submissions in China - Webinar
Жыл бұрын
Taking Advantage of the EU MDR Delay in Uncertain Times - Celegence Webinar
1:31:23
Taking Advantage of the EU MDR Delay in Uncertain Times - Celegence Webinar
Жыл бұрын
Celegence EUMDR Webinar - How To Start Preparing Your RA QA Team For The EUDAMED Database
1:05:04
Celegence EUMDR Webinar - How To Start Preparing Your RA QA Team For The EUDAMED Database
Жыл бұрын
Clinical Evaluations for Unique Product Types Under the EU MDR - Webinar
1:29:01
Clinical Evaluations for Unique Product Types Under the EU MDR - Webinar
Жыл бұрын
Best Practices for UDI Implementation and EUDAMED Submissions - Webinar
1:18:55
Best Practices for UDI Implementation and EUDAMED Submissions - Webinar
Жыл бұрын
Пікірлер
@MTB_Rider_96
@MTB_Rider_96 7 ай бұрын
can a product made up of two 510k cleared medical devices and no biologics or drugs be classified as a combination device?
@exploreyourdreamlife
@exploreyourdreamlife 10 ай бұрын
Your explanation of the effects of EU MDR extension are truly effective. Thanks for being such a great teacher! Liked and Subbed!