Emerging life sciences companies often face complex product registration processes and challenging interactions with Health Authorities (HAs). Compliance requirements vary across regions, making global submissions time-consuming and resource-intensive. In fact, a 2022 World Class RIM study by Gens & Associates found that 41% of small and very small life sciences companies rank Submission Planning & Tracking and HA Commitments among their top technology priorities.
In this on-demand webinar, learn how leading companies are leveraging technology to simplify product registration, improve compliance, and accelerate time-to-market. Our industry experts share real-world strategies covering:
- Performance Challenges at Emerging LS Companies
- Current RIM Landscape
- Modernizing Product Registrations with Technology
- Live Q&A
Access on-demand video
Speakers:
Preeya Beczek
Panelist
Independent Regulatory Affairs Expert
Beczek.COM Ltd.
and
Gens & Associates Partner
V. “Bala” Balasubramanian
Panelist
Life Sciences Practice Leader
Orion Innovation
and
RIM Reference Model Lead
DIA
Kevin Johns
Moderator
Director of Life Sciences Business Development
Orion Innovation
Who should watch:
This on-demand webinar is designed for Life Sciences and medical devices industry executives (VPs, Directors, etc) across all functions that interact with the regulatory lifecycle:
- Performance Challenges at Emerging LS Companies
- Current RIM Landscape
- Modernizing Product Registrations with Technology
- Live Q&A
Access on-demand video
Industries
Healthcare & Life Sciences
July 26, 2022
