Book Your Demo

See Litewave run on your own records and system data

Not a slide deck. Bring something you actually execute, a batch record, a stack of supplier certificates or an open deviation, and we will show you what Litewave finds in it and what it cites as evidence.

What we will walk through

• Reviewing every batch end to end, in hours rather than days
• Investigating deviations with the site history attached
• Checking incoming CoAs against your specification
• Checking your SOPs and QMS against the regulations you are held to
• Trending quality across sites and suppliers

Whether your records are on paper, in an eBPR or MES, or spread across both, and whichever standard your site is inspected against, from GMP and 21 CFR Part 111 to FSMA and ISO 22716.

Litewave is advised by former FDA investigators and by a Qualified Person who certifies batch release under EU GMP. They advise in a personal capacity, and FDA does not endorse products or companies.