Bringing your biologic to clinic
Avoid delays by being prepared to make the right decisions at the right time.
Getting regulatory ready
Navigate regulatory policies effectively and achieve regulatory compliance efficiently with discerning strategies for drug study, review, and approval.
Planning for IND
Learn how to navigate regulatory requirements as you progress through clinical trials to commercialization.
GMP manufacturing: where?
How to decide whether manufacturing in-house or outsourcing to a CDMO makes more sense for your product, process, and team.
Attract and keep skilled talent
What strategies should your company consider for recruiting, training, and retaining qualified candidates?
Cell therapy supply chain
A cell therapy’s success hinges on overcoming the challenges of manufacturing and administering a complex product.
Ballroom manufacturing with process closure
A ballroom facility design minimizes footprint, engineering, construction costs, and time to completion.
In-house or outsource
The decision to build a plant or outsource to a CDMO does not have to be mutually exclusive.
Cell and gene therapy development
An experienced contract development and manufacturing organization (CDMO) can ease scaling and tech transfer.
No more islands of automation
Improve overall efficiency of your operations by aligning procurement, finance, production, and other functions.
Podcast series
Listen to emerging biotech leaders as they weigh in on the latest important industry topics.
Biomanufacturing capacity
Addressing the need for flexible manufacturing options aligned with your business strategy
Scaling processes
Minimize chemistry, manufacturing, and control (CMC) risk without compromising quality or efficacy