VaxEng provides support to design and construct facilities that meet regulatory requirements for vaccines and biologics manufacturing. From URS to IQOQ, you can trust to support your engineering teams.

VaxEng provides support to transfer technology from one site to another at various stages from development to commercial production.

VaxEng provides support in process validation, process performance qualification, mixing and hold time studies, filter and E&L assessment.

VaxEng provides support in cleaning validation of process equipment to ensure consistent residue removal and meet quality standards.

VaxEng provides support in preparation of pre-approval inspection and health authorities inspection to ensure regulatory compliance.

VaxEng provides CDMO oversight services to guide clients from CDMO selection, due diligence, contract negotiation, technology transfer, manufacturing and regulatory filing.