Quality

Quality & Testing Centre

This page describes exactly how a batch becomes documented, which data we record, and what we will not say until evidence exists.

Verify a batch COA library

Batch records held

Batches with a published COA

Awaiting documentation

Counts are generated from the batch dataset — they are not marketing figures

Workflow

From incoming lot to public record

Four stages, each of which must produce a document before the next claim is made.

Batch intake and identification

Every incoming lot is recorded against a unique Ascetic Pharma batch identifier. That identifier is printed on the label and is the key used by every other record on this site.

Analytical testing

Batches are submitted for chromatographic purity analysis (HPLC) and mass-based identity confirmation (LC-MS). Residual moisture by Karl Fischer is recorded where the laboratory performs it.

Documentation review

A report is only attached to a batch when the report itself states the batch, the method, the date and the laboratory. Reports that cannot be matched to a physical lot are not published.

Release and public record

Once documentation is attached, the batch appears in the COA library and resolves through the verification page. Until then the record reads 'Pending verification' rather than showing a number.

Data model

What a batch record contains

Any field without evidence stays empty and renders as pending. No placeholder percentages, laboratories or accreditations are ever generated.

Batch / lot ID: Unique identifier printed on the vial label.
Product / compound: The catalogue entry the lot belongs to.
Status: Pending, verified, failed or archived.
HPLC purity: Reported percentage — blank until a report exists.
LC-MS identity: Observed mass / identity confirmation — blank until reported.
Residual moisture (KF): Optional, recorded only when tested.
Test date: Date the analysis was performed.
Laboratory: Name of the testing laboratory.
Accreditation / reference: Report reference supplied by that laboratory.
COA document: Link to the report file when published.
Release date: Date the batch was released against its documentation.
Notes: Anything that qualifies the record.

Current state

Batch register

The complete register, including records that are still awaiting laboratory documentation.

Ascetic Pharma batch register
Batch	Compound	HPLC	LC-MS	Status
AP-2401-A1	BPC-157 10 mg	—	—	Pending verification
AP-2402-B2	TB-500 10 mg	—	—	Pending verification
AP-2403-C3	GHK-Cu 50 mg	—	—	Pending verification
AP-2421-U3	GHK-Cu 100 mg	—	—	Pending verification
AP-2404-D4	Ipamorelin 10 mg	—	—	Pending verification
AP-2405-E5	Tesamorelin 20 mg	—	—	Pending verification
AP-2406-F6	Retatrutide 40 mg	—	—	Pending verification
AP-2407-G7	Selank 10 mg	—	—	Pending verification
AP-2408-H8	Melatonin 2 10 mg	—	—	Pending verification
AP-2409-I9	GLOW 70 mg Blend	—	—	Pending verification
AP-2410-J1	Kisspeptin 10 mg	—	—	Pending verification
AP-2411-K2	PT-141 10 mg	—	—	Pending verification
AP-2412-L3	Glutathione 1500 mg	—	—	Pending verification
AP-2413-M4	SNAP-8 10 mg	—	—	Pending verification
AP-2414-N5	KPV 10 mg	—	—	Pending verification
AP-2416-P7	Vitamin B12 10 mg	—	—	Pending verification
AP-2417-Q8	Melatonin 1 10 mg	—	—	Pending verification
AP-2418-R9	Melanotan 1 10 mg	—	—	Pending verification
AP-2419-S1	Melanotan 2 10 mg	—	—	Pending verification
AP-2420-T2	NAD+ 100 mg	—	—	Pending verification

What we deliberately do not claim

· No purity figure is stated anywhere without a matching laboratory report.
· No accreditation, ISO standard, certification or regulatory approval is claimed.
· No laboratory is named until it has issued a report we hold.
· No blanket "99 %+ every batch" statement is made.
· No therapeutic, diagnostic or human-use claim is made for any material.

Research and educational information only. Materials listed on this site are laboratory research materials. These records do not imply marketing authorisation or consumer-sale status, and the materials are not for human or veterinary use.