Quality Assurance

Reed-Lane prides itself on creating the highest quality pharmaceutical packaging products available. To ensure this standard, our organization is structured from the head down with an eye on quality. In addition to a full staff of quality assurance managers and production floor supervisors, our quality assurance director reports directly to our president. Remaining focused on the strength of our products has kept Reed-Lane on the cutting edge of healthcare packaging.

In the pharmaceutical packaging industry, quality can only be achieved through strict compliance with FDA and DEA regulations.  This thinking is why Reed-Lane has been a Current Good Manufacturing Practices (cGMP) compliant facility for decades. As part of its Quality Assurance Program, Reed-Lane requires that all employees receive extensive GMP training and that standard operating procedures be regularly updated to reflect current compliance protocols.  This guarantees that we don’t simply meet regulatory expectations for agencies and customers; we surpass them.

Reed-Lane not only complies with cGMP and the Code of Federal Regulations 21CFR 210 & 211, it also receives regular quality audits by the FDA and our customers. During the most recent 2006 FDA audit of the Reed-Lane facility, no specific references to any customer or product were made nor were any 483 observations made.

Reed-Lane also provides complete pharmaceutical validation services. These include validity of qualifications, protocol preparation, and installation and operational performance.