Webinar - Productivity Cost-Effective CER Writing - Celegence - Shruti Sharma

Cost-Effective CER Writing and Maintenance – Webinar

Webinar Background

How will you maintain your CERs without continuously adding new resources to your team and with confidence in your process and data?

Celegence’s innovative platform CAPTIS can reduce the time it takes to complete Systematic Literature Reviews for a CER, or a Literature Search Report while ensuring the highest level of accuracy. With a variety of time saving and collaboration features, Celegence has your end-to-end solution for faster clinical evaluation plans and reports.

This featured presentation will be led by Celegence’s Clinical Evaluation Report (CER) Expert, Shruti Sharma, who will also be available afterwards for a live Q/A.

Celegence will be hosting the WEBINAR on Wednesday, March 30th at 9 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.

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Webinar Featured Presenter – Shruti Sharma

Shruti Sharma has 6 years of experience in Medical writing, specializing in Clinical Evaluation Plans (CEPs), Clinical Evaluation Reports (CERs), Summary of Safety and Clinical Performance (SSCP) Reports, and Post-Market-Surveillance Reports (PMSRs). She has been the lead author for Clinical Evaluation Plans and Reports (CEP/CER) for device families across a wide range of therapeutic areas – endodontics, prosthodontics, diagnostic imaging, interventional neuroradiology, cleaning, disinfection, and sterilization devices, in addition to Software as a Medical Device (SaMD).

Webinar - Productivity Cost-Effective CER Writing - Shruti Sharma

Webinar Focus

This webinar will cover key features offered by CAPTIS Technology Solution which include:

  • Literature Search Database integration and simplified article management
  • Feature-rich Systematic Literature Review workflows for enhanced productivity
  • Source documentation management ensures information is consistently represented across your PMS related reports
  • Integrations with US FDA MAUDE and TPLC
  • Document lifecycle management for maintenance of CERs, PMCF reports, PMSRs, etc.
  • Collaboration among project managers, writers, and subject matter experts

Webinar Learning Objectives

  • Learn how the CAPTIS solution can allow your team to streamline all aspects of your PMS documentation and avoid constant revisions
  • Understand how the CAPTIS solution can reduce the time it takes to author your clinical documentation by nearly 20%
  • Examine examples and relevant case studies
  • Have your most pressing questions answered during the Q/A session

Who Should Attend?

This webinar is aimed towards those working for companies in the life sciences industry, particularly manufacturers of medical devices & IVDs, with a special emphasis on:

  • Regulatory Affairs Professionals
  • Quality Assurance Professionals
  • Medical Device Executives
  • Technical Writers and Managers
  • Medical Device Design Managers
  • Clinical Managers
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

Productivity Improvements for Cost-Effective CER Writing and Maintenance webinar will be held on Wednesday, March 30th at 9 am EST. Make sure you secure your spot at the webinar by registering now.

Webinar Signup - Cost-Effective CER Writing Celegence

Celegence – CER Services and Solutions to Support the Life Sciences

To learn more about our cost effective software for CER writing and maintenance then reach out to info@celegence.com or contact us online to schedule a demo! We are happy to share our insights with you during this webinar and hope that you can join us then

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