Rapid Expansion of Data-driven Chemical Development Through the Combination of Laboratory Automation, DoE and Modeling Techniques

The design, development and implementation of a robust, predictable, and scalable manufacturing process is the key outcome of chemical development. In chemical development, laboratory automation plays an important role—enabling the collection of large experimental arrays directed towards the discovery and optimization of process conditions that yield robust, predictable, and scalable manufacturing processes. To take a relevant example, rationally-designed and automatically-executed experiments can be used to accelerate the discovery of new reactions and build unprecedented understanding around chemical reaction dynamics.
Watch Now

Spotlight

OTHER ON-DEMAND WEBINARS

Transitioning Chemical Specialties from Clinical to Commercial in Small Molecule Drug Synthesis

Merck Millipore

In this webinar, we will explore best practice approaches for seamless handover at critical junctures en route to commercial manufacturing of small molecule drugs. One of the biggest challenges in today's small molecule drug development are the different requirements on quality and supply chain going from exploratory research to commercial manufacturing. A key risk to consider is the over- and/or underengineering of chemical specialties for drug synthesis leading to higher total cost of ownership.
Watch Now

Digitalization at Chemical Companies: Choosing the Right IT Solution as an Enabler of Growth

Sage X3

Live Webinar: Webinar Audio: You can dial the telephone numbers located on your webinar panel. Or listen in using your microphone or computer speakers. Welcome! Webinar Details • Presentation is roughly 1 hour • All phone lines are muted • If anyone has any questions during this webinar – please type them in your Questions Box located at the bottom of your webinar panel
Watch Now

Polymer Characterization Using Field-Flow Fractionation Combined with Multi-Angle Light Scattering

TFFFC is a platform dedicated exclusively to field-flow fractionation techniques used to characterizen macromolecules and nanoparticles.
Watch Now

CALIFORNIA HAZARDOUS MATERIALS BUSINESS PLAN (HMBP) REQUIREMENTS AND COMPLIANCE STRATEGIES

Verisk 3E

The California Hazardous Materials Business Plan regulations and compliance obligations can be complex and vary among regulating agencies. Utilizing Verisk 3E’s Regulatory Reporting Services team of actively involved, engaged and experienced regulatory professionals can be a highly efficient and effective way to alleviate the challenges associated with ensuring compliance with these complex and varying regulations.
Watch Now

Spotlight

resources