Mission Statement

Mission Statement

This is to certify that Simmler, Inc. has been a manufacturer of high quality blood bank reagents since 1968, subject to regulation by the Food and Drug administration, and is required to observe current good manufacturing practices in all aspects of its manufacturing and packaging operations.

Including, but not limited to:

1. The inspection and approval of all incoming raw materials to assure consistant compliance with predetermined and proven standards

2. Validated written manufacturing methods, proven to yield product safe for their intended uses.

3. In-process controls to maintain surveillance at all stages of manufacture

4. Documentation of all manufacturing steps and control results, with surpervisory review and approval to assure faithful observance.

5. Documented calibration of all measuring equipment and scheduled maintenance of machinery.

6. Periodical internal audits to confirm and maintain consistency of compliance.

7. Documented management of product complaints, with suitable testing when needed, to determine significant trends with product problems. All complaints and actions are reviewed at management level.

Our products are subject to licensing by the Food and Drug Administration, which regularly conducts inspection of the manufacturing and packaging premises.

After 35 years of business, Simmler, Inc. remains committed to the highest standards and quality at all levels of its operations, including research, quality control, manufacturing, packaging and customer service.

David P. Kremer

Vice President

Simmler, Inc.

P.O. Box 350

4564 North Square Dr.

St. Louis, MO. 63049

636-376-8347

800-325-0786

Fax: 636-376-8324