CAPA Form

An effective CAPA system requires many steps – documenting the source and effected systems, the investigation, the remediation, and the effectiveness check. This CAPA form free template will help initiate a CAPA for a non-conformity and capture all the information,...

CAPA Risk Assessment Form

Determining which non-conformity needs a CAPA is a complex process. Since not every non-conformity requires a CAPA, a thorough risk assessment should be put in place. This risk assessment free template will help you determine which non-conformity requires a CAPA based...

Calibration Log

This calibration log free template helps you capture the information needed to maintain an acceptable calibration record for your equipment, and will help comply with 21 CFR 820.72. Please fill out the form below to receive your calibration log free...

Approved Supplier List

This approved supplier list (ASL) free template will help you to keep track of which suppliers are approved for your company’s purchases. It is important to comply with 21CFR 820.50 Purchasing Controls and ISO 13485  section 7.4.1 Purchasing Process, which...

Complaint Form

Both the FDA and ISO emphasize customer complaint handling, so it’s important to formally record complaints. This complaint form free template can help document an incoming complaint and capture important information. Please fill out the form below to receive...