LAL Analysis

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Date

LAL Analysis: In accordance with FDA Guidelines and United States Pharmacopeia Guidelines

A.

Standard (10 units) (LAL)

B.

Standard Weekend (LAL-W)

C.

8-Hour Release (LAL-1)

D.

Re-test (LAL-T)

E.

Qualification (EIG)

F.

Quantify Pyrogen Level (LQN)

G.

Turbidimetric (TLAL)

H.

Chromogenic (CLAL)

Report Fees

A. Single formal reportOne formal report is included per test request. Additional reports are available.

One formal report (AR)

B. Fax documents and e-mail are available as follows:

1-2 pages (FX-1)
3-4 pages(FX-2)
5 and up (FX-3)

C. Weekend Fax

Weekend Fax (FXW)

Email

Electronic mail administrative service charge

Courier Services

B.I. Pick-up/delivery (C-1)
Other (C-2)
Additional (weekend) (C-W)

Product

On-Site Sampling Requested?

Yes
No
N/A

Chain of Custody to Accompany Samples? (EPA Requirement)

Yes
No
N/A

Professional Organizations