Free laboratory inventory, checklist and procurement worksheets

Lab inventory template excel: peptide tracking spreadsheet.

Download a lab supply order form, ready-to-use Excel workbook, peptide inventory CSV, field dictionary, receiving checklist and procurement templates for exact-product and exact-lot research records.

For qualified non-clinical research buyers. Not for human or veterinary use. The worksheet contains no administration, dosing, treatment or self-experimentation guidance.

What the template captures

One record another team member can reconstruct.

The worksheet keeps product, documentation, fulfillment and approval evidence together instead of scattering it across inboxes and screenshots.

IDENTITY

Exact product and SKU

Supplier, catalog name, SKU, lot, stated identity, format and quantity.

DOCUMENTATION

COA and lot match

COA location, lot match, report date, testing method and named testing source.

HANDLING

Storage requirements

Temperature plus any documented light, humidity or handling controls.

FULFILLMENT

Shipping and resolution

Method, cost, delivery window, refund terms and discrepancy contact.

COST

Comparable landed cost

Price-check date, unit price and total landed cost for a fair comparison.

CONTROL

Jurisdiction and approval

Jurisdiction check, reviewer, approval date and decision notes.

Lab inventory template Excel workbook

Use one file from procurement review through exact-lot close-out.

The downloadable .xlsx workbook keeps three distinct jobs in separate sheets: the purchasing decision, the receiving check and the ongoing inventory record. Filters, frozen headers and controlled status fields make the workbook immediately usable while leaving laboratory-specific procedures under local control.

INVENTORY SHEET

Twenty-six exact-lot fields

Track identity, quantity, format, lot, received label, documentation relationship, attributed storage statement, location, costs, local status, owner and final disposition.

RECEIVING CHECKLIST

Twelve evidence checkpoints

Review scope, identity, SKU, lot, quantity, format, package condition, documents, storage, costs, ownership and close-out without turning a checked box into a quality claim.

PROCUREMENT REVIEW

Keep the pre-order decision separate

Capture the exact seller title, listing date, current price, shipping, landed cost, availability, jurisdiction review and decision notes before a material enters inventory.

CONTROLLED STATUS

Make unresolved records visible

Dropdowns distinguish records that are not reviewed, held pending clarification, exceptions or locally released instead of silently filling gaps.

PORTABLE BACKUP

Keep the CSV options

Use the existing CSV downloads when a plain-text import or system-independent record is preferable to an Excel workbook.

QUALIFIED SCOPE

Inventory records, not use guidance

The workbook has no dosing, administration, injection, treatment, human-use or veterinary-use fields.

For qualified non-clinical research inventory and procurement only. Adapt the template to approved local procedures; the workbook does not verify product identity, quality, purity or experimental suitability.

Laboratory reagent inventory template

Keep receiving facts separate from purchasing assumptions.

The 22-field inventory CSV creates one row per exact received lot. It preserves the supplier and SKU, received label identity, quantity and unit, storage location, documentation match, package condition, local status, accountable owner and final disposition.

RECEIVING

Record what physically arrived

Capture the received date, exact visible label identity, supplier, SKU, lot, format, quantity and package condition.

TRACEABILITY

Use a stable internal ID

Assign one inventory identifier to the exact lot instead of relying on a nickname or a changing supplier page.

DOCUMENTS

Preserve lot-match status

Link the supplied document and state whether it exactly matches the received lot; leave unresolved fields unresolved.

LOCATION

Record storage facts

Keep the documented storage temperature, assigned location and applicable expiry or retest date with the lot record.

CONTROL

Use explicit local status

Record received, held pending clarification, released under the laboratory's process, returned or disposed—without turning status into a quality claim.

OWNERSHIP

Name the responsible owner

Track the person or function responsible for the record, last review date, disposition and any unresolved exception.

Worked inventory-row example

Translate a live listing into fields another researcher can audit.

This example uses one exact current research-use listing to show what belongs in a pre-order record. It is not a lot-release decision and does not replace the received label or batch-specific documentation.

GHRP-6 5mg product photograph supplied by BioPepTitech

GHRP-6 5mg

Exact identity
GHRP-6
Labeled quantity
5mg
Seller-listed format
Lyophilized Powder
Current price
$20.00
Live availability
Available
Seller storage statement
Refrigerated storage recommended

Facts checked 2026-09-22 against the live seller listing. Record the exact lot and match its current batch-specific documentation at receipt; PRX has not independently verified a public lot-specific certificate or the seller's analytical-verification statement.

Disclosure: We may earn a commission from purchases made through our links.

Save 15% on eligible purchases with affiliate code 15%OFF. Confirm eligibility in the seller cart.

View the exact GHRP-6 5mg listing Review GHRP-6 5mg procurement details

Qualified non-clinical research procurement only. This worked record provides no dosing, administration, injection, treatment, human-use or veterinary-use guidance.

Peptide tracking sheet and inventory spreadsheet

Track exact identity, quantity, lot and documentation without use instructions.

Use the downloadable CSV as a peptide tracking sheet, inventory spreadsheet or lot log for qualified non-clinical research operations. It keeps purchasing, receiving, storage-source and reconciliation fields in one auditable row per exact product and lot.

CATALOG IDENTITY

Keep the seller title and exact SKU

Record the supplier, seller product title, SKU or handle, stated compound identity, labeled quantity, quantity unit and seller-listed format as separate fields.

LOT TRACEABILITY

Match the received label

Capture the received-label identity, lot or batch identifier, receipt date and package condition instead of assuming the order record describes the delivered material.

DOCUMENT STATUS

State the COA relationship

Save the document location and mark whether it exactly matches the received lot. An unresolved lot match remains unresolved; a spreadsheet entry is not analytical verification.

STORAGE SOURCE

Preserve attributed instructions

Record the storage statement exactly as attributed to the current seller or supplied document, plus the assigned internal storage location and review date.

COST CONTROL

Separate unit and landed cost

Keep order quantity, listed unit price, shipping and landed cost distinct so procurement comparisons can be reconstructed later.

RECONCILIATION

Close exceptions explicitly

Assign a responsible owner, local inventory status, exception notes and final disposition rather than silently normalizing identity, quantity or document mismatches.

For qualified non-clinical research inventory control only. The spreadsheet includes no dosing, administration, injection, treatment, human-use or veterinary-use fields.

Peptide inventory sheet field guide

Reconcile four evidence sources without silently merging them.

A useful inventory sheet preserves what was ordered, what arrived, what the current seller page says and what the supplied document says as related but distinct records. The downloadable field dictionary defines all 26 columns in the inventory CSV.

ORDER RECORD

Freeze the purchasing facts

Keep supplier, exact product title, SKU or handle, listed identity, quantity, format, price and the page-capture date together.

RECEIVED LABEL

Record what physically arrived

Enter the received-label identity, lot or batch identifier, receipt date and package condition without overwriting the order record.

CURRENT LISTING

Treat catalog changes as new evidence

A current listing can help identify drift, but it must not replace the dated page or order evidence used for the original procurement decision.

SUPPLIED DOCUMENT

State the exact-lot relationship

Save the document location and classify the lot relationship as yes, no or unresolved. A filename or link alone is not a match.

EXCEPTION CONTROL

Assign every mismatch

Give identity, quantity, format, lot, document or condition discrepancies an owner, next action and final disposition.

HANDOFF READY

Make the row reconstructable

Another qualified team member should be able to find the source evidence, understand each unresolved field and identify the accountable owner.

For qualified non-clinical research inventory control only. These files organize procurement and receiving evidence; they do not verify identity, purity, quality, experimental suitability or any human or veterinary use.

Request for reagents or supplies

Lab supply order form for exact-product procurement

Use one row per requested seller listing. The 45-field CSV keeps the request, current listing, estimated commercial terms, approval, receiving evidence and discrepancy close-out in one reconstructable record.

REQUEST

Define the requirement first

Record the requester, research group or cost center, buyer jurisdiction, intended non-clinical context and required-by date before selecting a listing.

EXACT LISTING

Identify the material literally

Capture supplier, seller title, SKU or handle, exact identity, labeled quantity, unit, format and source URL without normalizing similar names.

COST & AVAILABILITY

Preserve the dated commercial snapshot

Keep unit count, current unit price, subtotal, shipping, fees, landed cost, discount eligibility and current availability as separate fields.

PRE-ORDER GATE

Resolve shipment and evidence questions

Confirm shipment eligibility for the buyer jurisdiction, request needed documents, state the document-to-lot relationship and preserve attributed storage and discrepancy terms.

APPROVAL & RECEIVING

Connect authorization to what arrived

Record approval status and owner, purchase-order or receipt identifier, received date, lot or batch, label identity, quantity and package condition.

EXCEPTION CLOSE-OUT

Assign unresolved discrepancies

Give each mismatch an owner and status, retain the evidence location and review date, and never silently rewrite the original order request.

Decision rule: approval should remain pending when exact identity, labeled quantity, format, buyer-jurisdiction shipment eligibility or required documentation is unresolved. A completed form does not establish quality, legal status or fitness for purpose.
For qualified non-clinical research procurement only. This order record contains no human or veterinary use guidance and no administration guidance.

Lab supply order form updated 2026-09-22 · 45 fields

Laboratory inventory checklist

Twelve checkpoints from scope to close-out.

Use the checklist as a starting control record, then adapt owners, frequencies, status terms and evidence requirements to your laboratory's approved procedures. A checked box is not evidence of identity, quality or experimental suitability.

SCOPE

Define the inventory boundary

Record which non-clinical research-material categories, rooms, freezers and cabinets are covered so omissions can be identified instead of assumed away.

IDENTITY

Keep one ID per exact lot

Connect the internal inventory ID to the supplier, exact product name, SKU, lot, received-label identity and format. Do not merge similar names or lots.

RECEIVING

Reconcile ordered and received records

Compare the purchasing record, packing record, physical label, quantity, package condition and supplied documentation as separate sources.

DOCUMENTS

State the lot relationship

Record the document title, location, date or revision and whether it exactly matches the received lot. Leave unresolved relationships unresolved.

CONTROL

Assign status and exceptions

Use laboratory-defined statuses and give every mismatch a category, owner, due date, evidence request and final disposition.

REVIEW

Close the audit trail

At each local review interval, reconcile identity, location, quantity, storage source, document status and downstream record updates.

At setup

Define scope, stable identifiers, status vocabulary, accountable owners and review frequency.

At every receipt

Record physical observations, compare exact identifiers, preserve document metadata and route discrepancies without silently correcting the source record.

During inventory use

Update quantity and location by exact lot while retaining transaction dates and responsible ownership.

At periodic review

Record what was checked, evidence consulted, corrections made and unresolved exceptions. Do not treat a current supplier page as a historical receipt record.

At close-out

Preserve return, disposal or other laboratory-authorized disposition, the decision owner, date and affected downstream records.

CSV preview

Twenty-six fields, no locked software.

Open the file in Excel, Google Sheets, Numbers or a laboratory procurement system that accepts CSV.

SupplierProduct / SKULot / COAMethodStorageLanded costApproval
Supplier nameExact catalog identityCurrent lot matchDocumented methodRecorded conditionsComparable totalReviewer + date

Suggested workflow

Use it before price decides the order.

Create one row per exact product and lot.

Do not merge different quantities, formats or lots into a single record. Carry the approved procurement identifier into the receiving and inventory record.

Link evidence instead of paraphrasing it.

Save the product page capture date and the exact COA or specification location reviewed.

Calculate landed cost after shipping.

Compare like-for-like quantities and include shipping or other disclosed order costs.

Reconcile at receipt.

Compare the order, received label, lot documentation and current listing as separate records. Hold discrepancies under the laboratory's procedure instead of silently normalizing them.

Record the final qualified reviewer.

Keep the approval date, jurisdiction check, responsible inventory owner and any unresolved limitation with the record.

Next procurement step

Compare current research formats and seller-listed prices.

After the documentation fields are defined, use the PRX comparison and reviewed catalog to shortlist eligible research-use listings.

Disclosure: We may earn a commission from purchases made through our links.
Compare research formats and pricesSearch the reviewed catalog

Commercial links on those pages are for qualified non-clinical research procurement only.

Evaluating a research-material supplier? Download the supplier audit checklist for Excel to record evidence, findings, owners and decisions.

For larger or repeat purchases: use the peptide supplier comparison checklist to capture tier quantities, lot allocation, landed cost and discrepancy terms before filling this record.