Supplement Brand Owner's Guides for Manufacturing Records

Ensure compliance with FDA Good Manufacturing Practices and regulatory requirements with proper record keeping and documentation.

At the heart of compliance with Good Manufacturing Practices and Quality Assurance records is good documentation. Use these guides and forms to help make sure nothing goes unrecorded.

Batch Documentation Form

A form to record and validate information regarding a manufacturing batch run of a dietary supplement.
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Batch Quality Assurance Guide

A guide for brand managers and QA representatives to ensure proper manufacturing documentation for dietary supplements and related products
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Manufacturing Documentation Guide

A guide for the complete documentation of a manufacturing process
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These guides and forms can help you build a good set of Dietary Supplement Standard Operating Procedures for Supplement and Sports Nutrition Brands.  Contact us if you would like a referral to an experienced Quality Control Consultant who can help set up your SOPs to meet the exact requirements of your company.  Whoever sets up your SOPs should have QC and regulatory knowledge that is current with the ever-changing landscape in this industry.

The information provided on this website does not, and is not intended to, constitute legal advice or SOP’s; instead, all information, content, and materials available on this site are for general informational purposes only.

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ABOUT US

Crystal Systems delivers software and services for the natural food, dietary supplement, and personal care industries. In addition to software systems, the network of Crystal consultants provides specialized product development, quality assurance, and regulatory compliance consultants, and we can set up operational services for managing contract manufacturers and third-party logistics.

Park City, UT 84098