Giving Your Contract Drug Manufacturing a Fresh, More Productive Start
How we help set - and keep - your success in motion
A partner who can scale up and is primarily configured to manufacture both clinical and commercial supply.
A partner who is conveniently located to API suppliers, clinical trial locations, primary commercial markets, an experienced workforce, etc.
A partner who prioritizes the processes, culture, and/ or technologies to ensure consistent quality.
The company cultures are a good match (e.g., a client needs flexibility and the CDMO is agile enough to meet those needs).
A partner who has the capacity, capability, and track record to meet aggressive timelines.
A partner who can accommodate your preferred presentation — vials, syringes, liquid, lyophilization, etc.
They’ve just completed Phase I
They’ve used one CDMO for small-scale trials but need a partner with more robust capabilities for Phase II and beyond.
They’re about to start Phase III
They have to be able to run Phase III registration lots with their intended commercial supplier.
They have an approved product
Their product is already on the market and they need a commercial tech transfer to provide additional supply, secondary supply, supply in a particular geography, etc.
Let's Do Your Impossible
As your team unites to address your innovative therapeutic or vaccine, our team would welcome the opportunity to contribute our special capabilities to your efforts. Wherever your instincts and inspirations lead, we possess the experience, knowledge, and capabilities to support your program.
We can get started together with an initial assessment, viability analysis, or virtual or onsite tour. But often the best way to kickstart the process is with a conversation so we can get a better sense of your specific goals, unique needs, and key development drivers.
The sooner we connect, the sooner we can help put your product in the hands of patients who can benefit so greatly from it. So let’s start today.