CSLLC maintains an extensive library of standard operating procedures. These are available to purchase to clients. Data collection forms that are used to record quality data are also available for the SOPs that require them.
Procedures include:
-Internal Audits,
-Document Control,
-Change Control,
-Investigation of Process/Product Deviations (including immediate response to, and management of, deviations to minimize long term effect and risk),
-Managing Corrective and Prevent Actions (to assure the root cause is resolved),
-Managing an FDA Inspection,
-Complaint Handling,
-Management Review,
-Management Responsibilities,
-Control of Nonconforming Materials,
-Receiving,
-Purchasing procedures (including an approved supplier list),
-QA Responsibilities,
-Batch Record Review,
-Product Release,
-Supplier Approval and Qualification,
-Development of a Quality Manual,
-Sampling.
Use these SOPs to initiate a quality system or to fill gaps in an existing quality system. CSLLC will work with you to customize the content of the procedures so they work effectively in your organization.