Supplements · R&D
R&D software for supplement manufacturers
R&D software for supplement manufacturers. Blend trials, compression, capsule fill, stability and scale-up sit on the live formulation record, so lab work becomes a manufacturable specification.
Today
A blend that flowed perfectly at 5kg segregates at 400kg, and the trial history that would explain it's spread across notebooks and one technologist's memory.
Generic lab and project tools record that a trial happened. They don't hold actives, assay basis, overage, permitted forms, maximum levels or the cost the formulation has to hit, so feasibility is discovered late.
With Worldover
Worldover R&D connects blend trials, compression and fill data, stability and scale-up results to the formulation version, the material specifications and the brief they belong to.
Development output is a specification production can run and regulatory can defend, rather than a formulation that needs re-proving.
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 Thursday in the lab
The difference isn't another isolated tool. It's the same work running from one live record.
Where work breaks
Trials are stored, not connected
A shared drive records the result. It can't tell you the winning trial used a premix grade you no longer buy.
Cost and MOQ arrive after the science
Technologists optimise the dose, then find the active has a 250kg minimum order and a twelve-week lead time, so the work is redone.
Compliance is a gate, not an input
Permitted forms, maximum levels and claim wording are checked at the end, when change is expensive rather than free.
- 01
A customer asks for a vegan capsule version of an existing tablet at the same cost per serving.
- 02
Today: the technologist copies a spreadsheet, chases procurement for prices and asks regulatory whether the form is permitted in three markets.
- 03
In Worldover: the existing formulation is cloned as a new version with its cost, supplier and compliance context attached.
- 04
Candidate actives and excipients show price bands, MOQs, lead times and permitted forms while the technologist is still choosing.
- 05
Stability and dissolution results attach to the trial, and the version that passes becomes the released specification without re-entry.
With Worldover
- 1
Brief lands with its constraints
Target cost per serving, format, market and claim requirements are visible in the lab, not sitting in the commercial team's inbox.
- 2
Trials build on the product record
Every trial references the actives, grades and batches used, so results stay interpretable months later.
- 3
Stability and testing run to completion
Protocols, pull points and results sit on the version, with outstanding tests visible before anyone promises a launch date.
- 4
Scale-up carries the evidence forward
Pilot and production trials link to the same version, so problems at scale are diagnosed against known lab conditions.
Connected inside Worldover
One product workflow.Every consequence connected.
Formulation is substance work. Worldover stores active form, salt factor, assay range, allergen status, excipient function and permitted use on the material itself, so a technologist meets the constraint while choosing rather than at the review meeting.
Willow
Useful AI starts with live operational context.
Scoped permissions, human approval for anything material and a full audit trail of every action.
- Which trials used this premix grade, and what happened to dissolution when we changed it?
- What's the cheapest permitted form of this active that still meets the declared value?
- Which developments are waiting on stability pull points this month?
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.