Contract Manufacturing and Development Services

We offer Inventprise’s GMP manufacturing capacity, and world-class human resources for the production of clinical material up-to phase-1. Inventprise can work with you on bottom-up process development or specialized process optimization. In addition, we offer and end-to-end outsourcing opportunity that includes QC assays, batch records, a full set of documentation, and in-person training. We have worked with all kinds of organizations small and large, including corporate partners, non-profits, academic institutions and governments.

We will work with your existing process – we’re flexible and understand that each of our clients has special requirements.
Inventprise owns a fully equipped vaccine development and GMP manufacturing facility. Our 17,000 square feet of space includes certified BSL-2 areas for research, development and engineering, as well as class 10,000 or better clean rooms for GMP activities.

Our upstream and downstream process volumes range from 0.25L to 20L, and conjugation volumes range from 1mL to 2L. We have multiple bacterial and viral downstream technologies (continuous centrifugation, AKTA, TFF, homogenization, etc) to tackle different processes. We’re capable of handling both bacterial and viral products and all related clinical material manufacturing activities up to Phase 1.

To support our manufacturing activities, we have a fully equipped quality control lab for identity, potency, purity and stability testing. All of our GMP activities are strictly monitored by our quality assurance team and we’re fully compliant with all regulatory guidelines. Our facilities and critical equipment are under environmental monitoring for quality assurance purposes. Our cGMP warehouse and purchasing procedures aid in the creation of batch records for all of our GMP activities and provide end-to-end traceability.