Facility Tours

See how APEX CSM protects quality, label accuracy, and on-time execution across our FDA- & cGMP-certified network. Get a guided walk-through of production controls, in-process checks, packaging lines, and release documentation—so you can move forward with confidence.

QA & batch recordsRaw material controlsEncapsulation & tabletingPackaging linesLot traceabilityAudit-ready workflows
Request a Quote

Want a virtual tour, NDA-first, or a multi-site view? Include it in your request and we’ll route you to the right facility and team.

Bright, modern supplement manufacturing corridor with PPE signage, clean floors, and stainless equipment visible through glass

Why Facility Tours Matter for Brand Owners

A tour isn’t about the nicest lobby—it’s about verifying controls that protect your brand when you scale, enter retail, or sell through demanding marketplaces.

Trust the System

Walk through the checkpoints that support consistent weights, counts, seals, labels, and finished-goods release. You’ll see how SOPs translate into predictable outcomes.

Validate Documentation

Tour the workflow behind COAs, lot coding, traceability, and batch records—so your team can align expectations for audits, retailers, and internal QA reviews.

Confirm Scalability

See production capacity, line configuration, changeover discipline, and packaging options. That visibility helps you plan launches and replenishment schedules with fewer surprises.

Request a Quote

What You’ll See on an APEX CSM Tour

Tours are customized by dosage form and project needs, but most visits cover the same quality-critical stations—from receiving to release.

Review how ingredients and components are received, identified, and staged. We’ll walk through quarantine practices, sampling flow, and traceability expectations that help protect label claims and minimize deviation risk.

See the role of identity, potency, and contaminant screening in release decisions. We’ll also explain how your specifications translate into documentation, hold points, and batch disposition.

Tour the flow from calibrated weighing through blend verification and in-process checks. This is where uniformity, flow, and consistency get protected before anything enters a press, encapsulator, or filling line.

Based on your product, we’ll prioritize relevant areas such as encapsulation, tableting, powder blending and filling, gummy operations, liquid lines, and specialty systems. You’ll see how changeovers and sanitation align to quality expectations.

See counting, bottling, sealing, labeling, and case packing in action. We’ll cover lot coding, reconciliation, and label controls—critical for reducing relabeling risk and helping your product ship right the first time.

Packaging Formats You Can Explore on Tour

Most tours include a packaging walk-through so you can match your brand experience to operational realities and lead times.

  • Bottles, jars, and canisters
  • Pouches, stick packs, and sachets
  • Blister cards and multi-SKU kits
  • Retail-ready cartons and shipper configurations
QA specialist reviewing batch documentation at a workstation with a tablet, barcode scanner, and labeled sample containers in a clean lab

Tour Outcomes You Can Use Internally

Leave with clarity your team can operationalize—especially helpful for brands managing procurement, regulatory, and forecasting across multiple SKUs.

Quality Alignment

Agree on specs, documentation expectations, and release flow.

Lead-Time Inputs

Validate packaging choices and line fit to protect timelines.

Scale Planning

Understand capacity and changeovers as volumes ramp.

Risk Reduction

Spot potential pitfalls early—before you lock a launch date.

Request a Quote

How to Schedule a Tour

A clear path from request to walkthrough. We keep the process simple so you can make decisions faster.

1

Request

Tell us your dosage form, packaging, target ship date, and preferred tour format.

2

Match

We route you to the best-fit facility and team based on capacity and certifications.

3

Prepare

We confirm visitor requirements, PPE, photo policy, and any NDA or compliance needs.

4

Tour

Walk through stations most relevant to your project—production, packaging, QA, and release.

5

Next Steps

We align on specs, timelines, and a clean quote path to keep momentum moving.

Stainless steel supplement packaging line with conveyor, labeler, and tamper-evident sealing station in a clean, well-lit production room

Visitor Guidance for Smooth Access

Because tours operate within active manufacturing environments, we focus on safety and product protection. Your tour coordinator will confirm the facility-specific requirements.

  • Closed-toe shoes and appropriate attire (no loose jewelry)
  • PPE instructions and controlled-area entry guidance
  • Photo/video policy based on area sensitivity
  • Timeboxed route designed to keep production moving

Quality Systems You Can Expect to Discuss

Every brand has different risk tolerance and channel requirements. Tours can go deeper into the topics that matter most to your roadmap.

Specifications & Testing

Align on identity, potency, purity, and contaminant expectations—including how specs are documented and verified across batches.

Traceability & Controls

See how lot coding and reconciliation support traceability from incoming materials to finished goods and shipment records.

Changeovers & Sanitation

Understand how changeovers and cleaning procedures protect your product and help maintain consistent output at scale.

Packaging & Label Controls

Review how label accuracy, component verification, and line checks reduce relabeling risk and protect retail readiness.

Need a tour focused on a specific channel?

If you sell DTC, wholesale, retail, practitioner, or through strict marketplace requirements, include your channel in the request so we can prioritize the controls and documentation most relevant to your business.

Tour Formats

Choose the level of access that fits your timeline and stakeholders.

  • Virtual overview:fast, stakeholder-friendly, great for early qualification.
  • On-site walk-through:deeper operational visibility for decision makers.
  • Project-specific route:tailored to your dosage form, packaging, and scale plan.
  • Multi-site evaluation:compare options across our national footprint.

Fast Lead Times Start with Clear Inputs

To keep timelines aggressive, we’ll ask for the essentials up front—then map a realistic path to production.

  • Dosage form and target per-serving amounts
  • Packaging format and count configurations
  • Label status (draft vs final) and claim priorities
  • Target ship date and forecasted reorder cadence
Request a Quote

Facility Tours FAQ

Quick answers for planning, access, and what happens after your visit.

Yes. Virtual tours are ideal for early qualification, distributed teams, and faster scheduling. If you request a quote, note “virtual tour” and your dosage form so we can tailor the route.

Tours are based on operational availability and your project requirements. We prioritize showing the most relevant capabilities, controls, and packaging configurations for your product type and scale plan.

Bring your product concept details (dosage form, ingredient priorities, packaging format, target ship date). If you have a label draft, bring it too—your tour can include a discussion of label controls and documentation flow.

Policies vary by area and facility. Your coordinator will confirm what’s allowed ahead of time and on arrival so we can protect product integrity and operational confidentiality.

We align on next steps—specs, packaging options, documentation expectations, and a clear quote path. Then we map your timeline with a focus on fast lead times and flexible MOQs that support your launch and reorder cadence.

Ready to Tour and Build with Confidence?

Request a quote and tell us what you want to see. We’ll coordinate the right tour format and next steps for your dosage form, packaging, and timeline.

Request a Quote