Thermo Fisher Scientific™ is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer.
Producers of biopharmaceuticals are challenged to become more efficient in discovering and developing candidate drugs while assuring quality and increasing manufacturing productivity and reducing costs. Advanced instrumental techniques and analytical workflows can help to accelerate the development pipeline and optimize production processes.
Thermo Fisher Scientific has innovative solutions to support every stage of the bio/pharmaceutical process, from discovery through to production and QC. Our deep understanding of the challenges faced by scientists developing lifesaving medicines allows us to forge partnerships that more quickly deliver next-generation drugs to market.
Visit us at www.thermofisher.com/biopharma

You’re invited to join us in person in the Grand Ballroom at 1:00 p.m. on Tuesday, January 25th for our lunch technical program: Bringing MAM to the Next Level – presented by Yi Zhang and Hao Yang.
You’ll learn a holistic, compliance-ready MAM platform, Thermo Scientific MAM 2.0, that enables deployment of MAM across all stages of biotherapeutics development and manufacturing with seamless knowledge sharing at global scale.
The lab tour is self-guided with audio voiceovers in each room and contains video demonstrations of the full workflow from development to QC. There is also a learning center where you can discover MAM and MAM 2.0 along with access to the latest application notes, case studies and more.
OR
Register for our expert-guided virtual MAM 2.0 Software Demo Sessions by e-mailing belysia.walker@thermofisher.comwith your contact info and preferred session time.
Please note that there are varying capacities for each session. Our 45-minute session allows for 5 registrants; our 1 hour session allows for 8 registrants; and our 1 hour+ session allows for 10 registrants. You must be registered by 7:30 PM the previous day.
Please see below for session dates and times:
Date | Start Time | End Time | Sign Up Close Time |
1/26/2022 | 8:45 AM | 9:45 AM | Tues 1/25 at 7:30 PM |
1/26/2022 | 3:30 PM | 5:00 PM | 12:00 PM |
1/27/2022 | 9:00 AM | 10:00 AM | Wed 1/26 at 7:30 PM |
We offer SEQ rapid molecular methods for pharmaceutical manufacturing to help review the quality and safety of your pharmaceutical products, especially when accuracy and time-to-results are critical.
These methods detect impurities and identify contaminants by using molecular techniques such as DNA sequencing, PCR, and real-time PCR, and are fast becoming the standards for pharmaceutical analytics worldwide.
Learn more about our Contaminant and Impurity QC Testing

There’s no molecule too large or too small for this forum. Scientists, researchers, and analysts are all welcome.
Join in on the evolving conversations about biopharma and pharma challenges in the laboratory.