Taking Advantage of the EU MDR Delay in Uncertain Times – Webinar
Overview
Where
Online
When
10.00 AM EST
Webinar Background
IDMP data standards are forcing companies to capture more data than ever before – and effective data management can be time-consuming and costly. With the right technology and processes in place, organizations can get ahead of changing regulations and timelines, increasing their compliance agility, and minimizing expenditure risks.
Celegence will be hosting the webinar in partnership with ArisGlobal on Wednesday, December 15th at 10 am ET. Register online now here!
What You Will Learn
Webinar Learning Objectives
- The best practices for collecting, extracting, and enriching your data for submissions
- How to increase your cross-departmental business process efficiency
- Understand the ways we can support your journey through continued xEVMPD compliance, the multiple phases of IDMP compliance, UDI, and beyond.
Webinar Speakers
Vice President of Regulatory Services, Celegence
Lakshmeenarayana G Goundalkar
He is part of the Celegence leadership team focused on providing high quality solutions and services in the space of Regulatory Affairs. He has 18+ years in software product design, development, project management, implementation and SME consulting for global projects related to life sciences. LGG has successfully managed the global delivery teams for Regulatory services and support for 30+ pharmaceutical, medical device, and biologics companies.
Associate VP of Clinical and Regulatory Product Management, ArisGlobal
Sondra Pepe
Sondra Pepe leads product management for ArisGlobal’s Clinical and Regulatory solution portfolios. In this role, she is responsible for defining clinical and regulatory product strategies and roadmaps and overseeing the growth of the domains. Prior to ArisGlobal, Sondra gained nearly 20 years of experience in eClinical SaaS technology across a variety of companies and products, including leading roles in product management at Veeva and Medidata, working on CTMS, EDC and RTSM product sets.
Who Should Attend?
This webinar would support those working for companies in the life sciences, including pharmaceutical and medical devices, with a special emphasis on:
Quality and Regulatory
Product Development and Manufacturing
Engineering and Operations
Quality Assurance
Research & Development
Webinar Sign Up
Beyond Compliance: Preparing for IDMP now and into the future webinar will be held on Wednesday, December 15th at 10 am ET. Make sure you secure your spot at the webinar by registering now.
As regulatory specialists, we work across all phases of the product lifecycle from regulatory strategy, authoring, and all aspects of established product maintenance, including submission management, publishing, and health authority interaction. We leverage a global team of consultants to provide local regulatory insight, strategy, and intelligence. We are happy to share our insights with you during this webinar and we hope that you can join us then.
Authored By
Celegence Admin
Where
Online
When
10.00 AM EST
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