Real engagements.
Numbers, not adjectives.
Every case below is an actual engagement. Client names are withheld under NDA — full attribution available on request to serious buyers. What isn't anonymised: the metrics, the timelines, and the outcomes.
3 representative cases
Biocatalytic route replaces a hazardous reagent — 12 weeks to validated
An EU generics client needed to remove a controlled reagent from an existing route. Our R&D group delivered a biocatalytic alternative with equivalent yield in 12 weeks.
- Hazardous reagent removed
- Yes
- Yield vs. baseline
- Equivalent
- Timeline
- 12 weeks
- Downstream impact
- None
42% PMI reduction on a European specialty pharma molecule
A six-month route scouting engagement replaced a four-step literature route with a three-step biocatalytic alternative — halving solvent usage and clearing EU regulatory review at first attempt.
- Process mass intensity
- −42%
- Cost per kg
- −33%
- Timeline
- 6 months
- First-pass EU review
- Cleared
Site-to-site technology transfer: 4 months to a first-attempt PPQ pass
A validated 3-step API synthesis transferred from an EU-based CDMO to Operant Scientific with three consecutive PPQ campaigns cleared without deviations.
- Time to PPQ
- 4 months
- PPQ campaigns
- 3 of 3 pass
- Critical findings
- Zero
- Regulatory action
- None required
Want to talk to a reference?
For serious buyers evaluating a specific engagement type, we can arrange a reference call with the original client — subject to their consent. Send a two-line brief describing what you want to verify.