Beyond Compliance - Preparing for IDMP Now and Into the Future - Celegence ArisGlobal Webinar

Beyond Compliance: Preparing for IDMP Now and Into the Future Webinar with Aris Global

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 8th at 10 am EST. Register online now here!

EU MDR - Checklist - Celegence Life Science

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Make sure you and your business are compliant with the new EU MDR. Get our 23 page checklist for actionable technical documentation requirements.

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EU MDR - Celegence Life Science

Claim Your Free EU MDR Checklist Now!

Make sure you and your business are compliant with the new EU MDR. Get our 23 page checklist for actionable technical documentation requirements.

GET YOUR CHECKLIST NOW

Webinar Featured Presenters

  • Lakshmeenarayana G Goundalkar, Vice President of Regulatory Services, Celegence: 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.
  • Sondra Pepe, Associate VP of Clinical and Regulatory Product Management, ArisGlobal: 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.
  • Sonia Hurley, Senior Director Product Management, Regulatory, ArisGlobal: Sonia heads the Regulatory area of ArisGlobal’s Product Management team. Prior to joining ArisGlobal, Sonia acquired over 20 years of experience as a product visionary in the Life Sciences space in a variety of organizations. During her career, she acquired expertise with a number of highly regulated products in the Biotech/Life Sciences arena, applying principals focused on product management in the organization. Sonia currently resides in the Raleigh-Durham area and is a board member of ProductCampRTP®, and enjoys introducing newer product managers to formal methodologies for their product challenges. During her spare time, she enjoys traveling to different countries when the world is open.
Webinar Featured Presenters - Arisglobal - Celegence

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.

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
EU MDR - Checklist - Celegence Life Science

Claim Your Free EU MDR Checklist Now!

Make sure you and your business are compliant with the new EU MDR. Get our 23 page checklist for actionable technical documentation requirements.

GET YOUR CHECKLIST NOW
EU MDR - Celegence Life Science

Claim Your Free EU MDR Checklist Now!

Make sure you and your business are compliant with the new EU MDR. Get our 23 page checklist for actionable technical documentation requirements.

GET YOUR CHECKLIST NOW

Webinar Sign Up

Beyond Compliance: Preparing for IDMP now and into the future webinar will be held on Wednesday, December 8th at 10 am EST. 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.

Webinar Signup - IDMP Compliance - Celegence Arisglobal

Celegence – Services and Solutions to Support the Life Sciences

For more information on how Celegence can help improve your Regulatory Operations with Learning Management, reach out to us at info@celegence.com, contact us online or read more about Celegence’s regulatory operations capabilities.

For more information on how Celegence can help with Learning Management, reach out to us at info@celegence.com or contact us online