Supplements · R&D
R&D for food and supplement ingredient providers
R&D software for food and supplement ingredient suppliers. Application trials in tablets, capsules, powders and beverages feed the ingredient record sales and customers rely on.
Today
Your lab has already solved this customer's compression problem, for a different customer, two years ago, and nobody can find the work.
Electronic notebooks record experiments. They don't connect a dose-form trial to the grade it used, the customer who asked for it or the claim it ended up supporting, so application knowledge never becomes a commercial asset.
With Worldover
Worldover R&D connects application trials, dose-form work, stability and analytical results to the grade, the enquiry and the customer they belong to.
Application knowledge is found rather than recreated, and technical answers reuse work you've already paid for.
What's in it
What R&Ddoes inside Worldover.
The operational outcomes come first. Open any area to inspect the underlying controls, records and technical detail.
Standards and regimes
01R&D Lab SoftwareDigital lab covering raw materials, formulations and regulatory screening.
Raw materials workflow management
Build a raw material library with custom workflows across multiple material types, document types and field types, all defined by you during onboarding.
Composition management
Add ingredients to raw materials as ranges or exact percentages, with full impurities management at ppm.
Table management
Customisable views by coding system, part number, type or cost.
Complex cost management
Manage raw material costs with customisable costing modules, currency settings and automatic currency conversion.
Gap analysis
Reports showing which documents are present against which are missing.
Raw material administration
Codes and sub-codes to organise the library the way your team already thinks.
One workflow, end to end
A new dose-form request
The difference isn't another isolated tool. It's the same work running from one live record.
Where work breaks
Trials are filed by project, not by substance
The useful unit is the grade and the dose form. Filing by project buries both.
Results never reach sales
Solubility, flowability, compression and stability findings stay in the lab, so commercial teams answer from memory.
Stability data ages out of sight
Shelf life claims rest on studies nobody links back to the grade or the customer format they were run in.
- 01
A customer wants your active in a chewable, not a capsule.
- 02
Today: the lab starts from scratch because prior chewable work isn't findable.
- 03
In Worldover: prior trials on that grade and format surface with their results.
- 04
New work is logged against the grade and the customer enquiry that prompted it.
- 05
The findings feed the next technical response automatically.
With Worldover
- 1
Trials attach to the grade
Every application trial references the exact grade, lot and specification used.
- 2
Dose forms are first class
Tablet, capsule, powder, gummy and beverage work is tagged so it can be found by format.
- 3
Stability is connected
Studies link to the grade, the format and the shelf-life position they support.
- 4
Results become answers
Findings are visible to sales and service on the same ingredient record.
Connected inside Worldover
One product workflow.Every consequence connected.
Application work only compounds if it's attached to the substance. On one record, every trial makes the next technical answer faster.
Willow
Useful AI starts with live operational context.
Scoped permissions, human approval for anything material and a full audit trail of every action.
- What prior work do we have on this active in a chewable format?
- Which trials support the shelf life we quote for this grade?
- Summarise the compression findings for this grade across customers.
Buyer confidence
A specialist system, without a specialist-system rollout.
Worldover combines detailed operational control with a practical route to a live first phase.
- 50+
- Enterprise customers across cosmetics, chemicals and supplements
- 4 to 7
- Point systems typically retired, most within 6 months of go-live
- 12 to 16 weeks
- To a live Phase 1, not a multi-year programme
- 1 record
- Per substance, everywhere it appears
See it on your operation
Book a 30-minute slot
Give us the essentials, then choose a 30-minute slot directly in the right person’s calendar. We’ll use your workflow, products and documents, not a generic slide deck.