Thermo Fisher Scientific

To bring lifesaving cell and gene therapies to the market, an efficient and scalable manufacturing strategy is needed. Find out more in this whitepaper.

Download this whitepaper to get a better understanding of the evolving regulatory guidelines for cell and gene therapies, in order to bring them to market faster.

This whitepaper explores vaccine development during a pandemic, a response to complex challenges that traditional manufacturing methods won’t solve.

***Session 1: Thursday, April 22, 2021, 10am EDT, Session 2: Thursday, April 22, 2021, 11am EDT, Session 3: Thursday, April 22, 2021, 1pm EDT*** A drug’s journey from development to manufacturing to patients is paved with roadblocks and potholes; many threats can derail bio/pharmaceutical processes. Potential solutions to such pitfalls have been discussed for years; however, few manufacturers have embraced technology and process advances to proactively ensure drug supply chain continuity.

This application note demonstrates how to develop an analytical HILIC method and transfer it from an Agilent 1260 Infinity LC system to the Vanquish Core HPLC system.

Learn about the use of the MAbPac RP capillary column for utmost sensitivity and excellent selectivity for the mass spectrometric analyses of intact proteins and mAb subunits.

This work aims to develop and optimize a liquid chromatography (LC) ddMS2 method for the untargeted analysis of oligonucleotides using Orbitrap-based HRAM MS.

This white paper demonstrates a vendor’s perspective on recent trends in regulations and the potential future direction for the industry.

***Live: Wednesday, December 2, 2020 at 11am EST | 8am PST | 4pm GMT | 5pm CET***Learn more about the recent trends in single-use sensors to match bioprocessing needs of bioreactor, fermenters, and mixing applications. Review data from 2-year studies of sensor testing.***On demand available after final airing until Dec. 2, 2021***

*** Live: Wednesday, November 11, 2020 | 8:30 AM EDT – 4:00 PM EDT *** 2020 Bio/Pharma Virtual Congress: Join Pharmaceutical Technology® and BioPharm International® for this online event that will explore the latest developments in formulation, manufacturing, and innovative drug dosage forms, as well as detailed discussions about crucial topics impacting the industry. ***On demand available after final airing until 11/11/2021

This white paper will give readers a vendor’s perspective on recent trends in regulations and the potential future direction for the industry - being referred to as “Pharma 4.0”.

*** Live: Thursday, October 22, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST*** Be sure you’re using the latest XRD sample preparation and measurement strategies while confidently meeting audit trail and compliance requirements. Learn how recent software solutions enable straightforward, compliant pharmaceutical workflows. ***On demand available after final airing until Oct. 22, 2021***

Listen and learn as Dr. James Grinias from Rowan University and Dr. Frank Steiner from Thermo Fisher Scientific discuss approaches and considerations to modernizing HPLC methods to increase throughput using superficially porous particles. They also discuss challenges in method transfer and describe new compliant hardware technologies built into the modern HPLC and UHPLC systems. Live: Tuesday, Aug. 25, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing until Aug. 25, 2021

The promises of the digital lab are enticing but getting there can seem daunting. The good news is that you can start today. It’s simply about implementation, and not waiting for innovation. Live: Tuesday, Sept. 22, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST On demand available after airing until Sept. 22, 2021

An overview of data processing in the HR MAM workflow and demonstration of software for flexibility in different phases of drug development and manufacturing

Near infrared (NIR) spectroscopy to the rescue: See how this vital process analytical technology tool can improve efficiency and cut costs in your pharmaceutical QC processes. Live: Wednesday, Sept. 9, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Sept. 9, 2021

The Thermo Scientific Vanquish Duo system for Dual LC enables two sample runs concurrently, so samples to run in half the time, improving pharmaceutical drug analysis.

The Thermo Scientific Vanquish Duo system for Dual LC enables two sample runs concurrently, so samples to run in half the time, improving pharmaceutical drug analysis.

The Thermo Scientific Vanquish Duo system for Dual employs two separate flow paths for simultaneous analysis of complex samples.

This application note covers HRAM multi-attribute method for critical quality attribute monitoring and new peak detection, including optimization and application.

This application note covers HRAM multi-attribute method for critical quality attribute monitoring and new peak detection, including optimization and application.

This application note demonstrates the capabilities for Dual LC to run independent HPLC and UHPLC methods simultaneously using one instrument.

Discussion of the transfer of analytical HPLC methods from a Waters Acquity UPLC system to the Vanquish platform and highlights the impact of column thermostatting.

This application note demonstrates how sensitive UV detection provides quantitation of a genotoxic impurity at low ng/mL level.

Designing a formulation for a drug product calls for careful attention to both the physical and chemical properties of the active pharmaceutical ingredient. Find out how a pharmaceutical company can recognize both unfavorable drug substance properties and incompatibility between an API and its formulation to avoid potential risks to the patient and more.

ORC International’s report Implications of Inaccurate Forecasting on Biologics Drug Substance Manufacturing explores causes, consequences, and potential solutions to forecasting challenges related to biopharmaceutical drug substance manufacturing. It provides insight and perspective on key themes that emerge from the report, offering additional solutions to prepare for inevitable forecast inaccuracies.

Are you looking to ensure compliance to the latest demanding regulations? Do need to be able to easily demonstrate control of your data? With Thermo Scientific™ Chromeleon™ CDS software you can rest assured.

Join experts from SGS and Thermo Fisher Scientific to hear how to improve workflows for confident extractable and leachable studies. Live: North America: Tuesday, Oct. 31, 2017 | 11am EDT | 10am CDT / Europe: Tuesday, 7 Nov., 2017 | 9am GMT | 10am CET / On Demand available after airing until 7 Nov., 2018. Register free: http://www.pharmtech.com/pt_w/analytical

Elemental impurity analysis is vital for ensuring the safety of pharmaceutical products. With newly revised and modernized standards for elemental and organic impurities slated to take effect soon, developers must understand and be able to meet the newest analytical requirements. In this eBook, learn from experts at the US Pharmacopeia what drug companies need to know about USP and . Also learn about the use of atomic spectroscopy techniques and sample preparation procedures for elemental impurities analysis.