Submission guide
Seven steps from online submission to certificate of analysis. The first five are completed by the client; receipt, analysis and release are performed by the laboratory.
Process
Submission details
Enter the company and contact email, then each product: the name as labelled, SKU and lot number. Label names are matched to the compound tested, so a product sold as GLP-3 is tested as retatrutide.
Client
Program selection
Select Essential Release, Comprehensive Release or Performance Study. One program applies to every lot in a submission.
Client
Invoice review and payment
The full cost breakdown is shown by analysis, by lot and by fee. Nothing is charged before the invoice has been reviewed.
Client
Shipping packet
On completion the packet is shown on screen and as a PDF. It carries the submission ID, a sample ID for each lot, packing instructions and the receiving address.
Client
Packing and shipment
Mark each vial with its sample ID, bag each lot separately, place page one of the packet on top and ship with tracking early in the week.
Client
Receipt and analysis
Vials are reconciled against the packet and receipt is confirmed by email. Analysis begins once every lot in the submission has arrived.
QuantVera
Certificate release
One certificate of analysis per lot, issued by email and held on record. Each carries a QR code that confirms it is genuine and unaltered.
QuantVera
Shipment contents
Sealed vials, one lot per bag
The quantity required by the program, all from the same lot, unopened, each marked with its sample ID.
Page one of the packet
Placed on top of the contents. It links the shipment to the submission.
Temperature
Lyophilised product ships at ambient temperature. Product in solution ships cold, overnight.
Begin a submission
The online form takes a few minutes per lot.