How Our Reagent Lyophilization Partnership With IDT Benefits You
As point-of-care (POC) diagnostics and high throughput sequencing expand in popularity, the need for room temperature-stable products grows. POC diagnostics need to be capable of
Year: 2019
How to Minimize API Loss: A Case Study in Aseptic Fill/Finish
With API (active pharmaceutical ingredient) values continuing to climb as production scales conversely drop, it is time to rethink our aseptic filling processes to minimize
Argonaut Manufacturing Services Announces Addition to Board of Directors
Mark O’Donnell Joins Argonaut Manufacturing Services Board Carlsbad, CA, Nov 05, 2019 – Argonaut Manufacturing Services announced today that Mark O’Donnell has been appointed to
When is the Right Time to Select a Biotech Contract Manufacturer (CMO)?
Every journey to contract manufacturing is unique. Some biotech companies know, at the start, they want to work with a contract manufacturing organization (CMO), while
Make Versus Buy: Evaluating your Aseptic Fill/Finish Manufacturing Strategy
Every biopharma company is eventually faced with the “make versus buy” decision – should they fill/finish their drug product in-house or outsource? Complicating things further,
Scale-up and Automation Strategies in Life Science Manufacturing
Scale-up and automation in life science manufacturing is challenging. When picturing a manufacturing line, you likely conjure up images of automated multi-function equipment or deft
Protecting Your Life Science Cold Chain From Styrofoam Bans
Life science companies, from reagents to diagnostics, rely on cold chain shipping. A vital component in the chain is the ubiquitous polystyrene cooler. Yet, with
Strategic plays to grow your biotech startup
Being a biotech startup is exciting. Your company is young, energetic, and full of potential. However, your company is likely lacking in two key areas:
New manufacturing strategies for the precision medicine future
Blockbuster drugs and one-size-fits-all treatments now share portfolio space with highly targeted therapies for smaller patient populations. This new era is an opportunity for savvy
How QSR-Compliant Medical Device Companies Can Switch to ISO 13485:2016
For decades, there has been a divide in the medical device regulatory landscape. While the U.S. Food and Drug Administration (FDA) has considered their Quality