Regions
MAIN/REGIONS
regions/
Regions
  1. Americas
  2. Asia & Oceania
  3. Europe
  4. Middle East & Africa
  1. Insights
  2. Events
  3. About
  4. Contact Us
MAIN/search
MAIN/Insights
Insights/
Our Latest Whitepapers

Get the latest insights on our life sciences, healthcare, and medical technology solutions in Asia Pacific. 

Learn More
Blogs, Case Studies & Podcasts

Explore our library of insights, thought leadership, and the latest topics & trends in healthcare.

Discover Insights

IQVIA APAC Insight

"A curation of IQVIA's best thinking on topics and trends driving change, disruption, and progress in the Asia Pacific healthcare market.

Read The Latest Issue
MAIN/Events
Events/
Upcoming Events & Webinars

View our upcoming events and webinars.

Explore The Latest
On-Demand Webinars

Visit our library of on-demand webinars.

Discover Insights

Featured Event

"Unlocking the Future of Consumer Health: A Special Focus on Senior Consumers

Learn More
MAIN/About
About/
Newsroom

Read the latest updates and press releases.

Learn More
Career Opportunities

Improving human health requires innovative thinkers who are willing to explore new ideas and build on successes. Unleash your potential with us.

Search Jobs

APAC FOOTPRINT

"Explore our Asia Pacific locations.

Learn more
MAIN/Contact Us
Contact Us/
Webinar
Navigating regulatory pathways in the US for Cell and Gene Therapy
calendar

October 28, 2021

Calendar
clock

11:00am - 12:30pm

GMT

WATCH ON-DEMAND

View all IQVIA events
View now

In recent years, Cell and Gene Therapies (CAGT) has seen tremendous growth in the Japan and Asia Pacific (JAPAC) region with a continually increasing number of biopharmaceutical companies initiating clinical trials with their innovative therapies.

As these Asia Pacific-originated programs progress, to maximize their return on investment, companies are beginning to look for ways to expand development and registration of their assets to the United States, the world's largest healthcare market.

Watch our on-demand webinar to discover how IQVIA can help you navigate the US FDA regulations of regenerative medicine therapies, take advantage of expedited programs and proactively address Chemistry, Manufacturing and Controls (CMC) considerations and ultimately increase the probability of your success.



Speakers

Monica R. Shah, MD, FACC
Vice President and Head, Cell and Gene Therapy Center of Excellence
IQVIA

Hardeep Samra
Sr. Director, Head of Regulatory Strategy, Strategic Drug Development
IQVIA

Eugene Brandon
Sr. Director and Head of Translation, Cell and Gene Therapy
IQVIA

Susan McClatchey
Sr. Director Product Development, Cell and Gene Therapy
IQVIA

Kristin Baird, MD
Medical Strategy Lead, Cell and Gene Therapy
IQVIA

Contact Us