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Why GIH ExistsHow It WorksThe GIH MethodInside the Facility

What We Build

Custom Formulation & R&DPrivate Label ManufacturingGummy ManufacturingTesseract TechnologyQuality & NSF GMP3PL & Fulfillment

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Modern pharmaceutical manufacturing facility interior

The six stages

How your product gets made, step by step.

Six stages, each one informing the next. The value is not that the steps exist — every manufacturer has steps. The value is that all six happen inside one company, so nothing is renegotiated at each handoff.

01

Discovery & product brief

We define format, what you are legally allowed to claim, target customer, channel needs, budget and timing — focusing on commercial objectives across product types and sales channels. You leave with a brief that guides every downstream decision.

  • Commercial objectives identified
  • Sales channel requirements analyzed
  • Budget and timeline established
  • Product format decisions made
  • Market urgency and promotional calendars considered

02

R&D + formulation

The company develops ingredient strategy, dosage specifications and flavor considerations while assessing feasibility before production launches. Guided by the best scientific knowledge at every formulation stage.

  • Ingredient strategy development
  • Dosage specification
  • Flavor considerations and optimization
  • Formulation feasibility assessment
  • Optional Tesseract delivery integration

03

Sourcing & compliance review

GIH aligns production inputs with quality standards and regulatory requirements, managing supplier expectations and label compliance so nothing surprises you at print or at customs.

  • Ingredient sourcing and supplier vetting
  • Quality standard alignment
  • FDA and GMP regulatory verification
  • Label claim substantiation
  • Cost structure optimization

04

Production run

Controlled manufacturing environments turn approved formulas into finished product, using specialized equipment such as gummy kettles and capsule machines across a facility that runs multiple shifts without downtime.

  • Format-specific equipment selection
  • Production scheduling
  • Batch documentation
  • In-process quality monitoring
  • Temperature and humidity control

05

Quality review & release

The facility implements documentation and in-process verification steps to ensure batch integrity before packaging or fulfillment. Nothing moves forward on assumption.

  • Documentation review
  • In-process verification
  • Quality checkpoint completion
  • Batch release decision
  • Record maintenance and traceability

06

Packaging, inventory & 3PL

Final stages encompass product presentation, warehouse management and fulfillment support — in the same building, by the same team that made it.

  • Packaging application and label verification
  • Inventory organization and product code management
  • Safety stock and reorder trigger setup
  • ShipStation integration and carrier coordination
  • Bundle configuration and channel prep

Decision points

Where you actually make choices.

Transparency about when input is needed from you, so the timeline never stalls waiting on an unasked question.

  • Format selection — gummies, capsules, powders and beyond
  • Technology integration decision — Tesseract versus standard delivery
  • Timeline establishment against your launch or promotional calendar

  • Ingredient approval
  • Dosage confirmation
  • Flavor and texture decisions
  • Technology application decision

  • Supplier confirmation
  • Cost structure approval
  • Compliance path confirmation
  • Label strategy finalization

  • Batch approval
  • Quality level verification
  • Volume confirmation

  • Final approval for packaging
  • Lot documentation finalization
  • Fulfillment readiness confirmation

  • Channel-specific packaging preparation
  • Inventory allocation
  • Fulfillment coordination

Timeline

Roughly what to expect.

Formulation & R&D

Typically 2–4 weeks depending on complexity and the number of iterations required.

First production run

Typically 4–6 weeks including formulation. Can be expedited when a launch date demands it.

Reorders

Typically 3–4 weeks once a formula and packaging are established and proven.

A clear path from formula concept to finished product.

The purpose of the six stages
Supplement bottle in dramatic golden-hour light

Let's build together

Stage one starts with a conversation.

Share the idea, the format, the channel and the timeline. We'll tell you what it takes to build it properly — and what it costs.

Or email info@gihlifesciences.com — we reply in 1–2 business days.

Ready to build? We reply in 1–2 business days.

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