Skip to content
GMPDocs.com logo
  • Home
  • About
  • Document Shop
  • Blog
  • Contact Us
  • WooCommerce My Account
    • Register
  • WooCommerce Cart0
    • WooCommerce My Account
      • Register
    • WooCommerce Cart0

      GMP Procedures (SOPs)

      • Sort by Default Order
        • Sort by Default Order
        • Sort by Name
        • Sort by Price
        • Sort by Date
        • Sort by Popularity
        • Sort by Rating
      • Show 12 Products
        • Show 12 Products
        • Show 24 Products
        • Show 36 Products
      • Audits and Reports

        View Cart

        Audits and Reports

        $39.95

        Procedure on how to perform audits and requirements for subsequent reports.

        View product
      • Batch Record Review

        View Cart

        Batch Record Review

        $39.95

        Batch records are commonly also known as: production records, manufacturing records. Whatever your firm calls them, you need a procedure on how review such records and record that review. This procedure describes how to effectively review batch records and document the review on the appropriate forms. During the review of batch records, it’s helpful to have a checklist to guide you along the way.

        View product
      • Batch Record Review Checklist Template/Example

        View Cart

        Batch Record Review Checklist Template/Example

        $4.95

        This document is an example Batch Record Review checklist.  It provides a proper template for how a well-designed checklist could work.  We recommend this document in conjunction with our Batch Record Review SOP.

        View product
      • Certificate of Analysis Package

        View Cart

        Certificate of Analysis Package

        $9.95

        Certificates of Analysis are required documents for most batches to be QA Released by an organization. This product contains 2 templates for a Certificate of Analysis. The first document is just a blank template/shell for a properly and cleanly formatted CofA. The second document is a filled in example template with example tests and result specifications for a typical biopharmaceutical product.

        View product
      • Corporate QA Audits

        View Cart

        Corporate QA Audits

        $39.95

        Procedure identifying the responsibilities and requirements for performing QA audits of operations related to the items that the firm/function oversees. This audit procedures applies to a higher / “corporate” level of oversight.

        View product
      • Corrective and Preventative Actions (CAPA)

        View Cart

        Corrective and Preventative Actions (CAPA)

        $49.95

        Procedure on corrective and preventative actions (CAPAs). Covers how to investigate for root cause, tracking of implementation of correction actions, and closure.

        View product
      • Creation of Forms

        View Cart

        Creation of Forms

        $29.95

        Procedure on how to write and the requirements for forms used with SOPs and other controlled systems.

        View product
      • Creation of Installation Qualification Protocols

        View Cart

        Creation of Installation Qualification Protocols

        $49.95

        Procedure on how to write and the requirements for equipment installation qualification (IQ) protocols.

        View product
      • Creation of Item Specifications

        View Cart

        Creation of Item Specifications

        $39.95

        Procedure on how to write and the requirements for Item Specifications.

        View product
      • Creation of List Documents

        View Cart

        Creation of List Documents

        $29.95

        Procedure on how to write and the requirements for simple list documents.

        View product
      • Creation of Logs and Logbooks

        View Cart

        Creation of Logs and Logbooks

        $29.95

        Procedure on how to write and the requirements for logs and logbooks used to support controlled systems.

        View product
      • Creation of Operational Qualification Protocols

        View Cart

        Creation of Operational Qualification Protocols

        $49.95

        Procedure on how to write and the requirements for equipment operational qualification (OP) protocols.

        View product
      12Next

      Product categories

      • FREE Documents!
      • GMP Procedures (SOPs)
      • GMP Quality Policies
      • Laboratory SOPs
      • Validation SOPs & Templates

      More about GMPDocs.com

      Your quick and affordable source for GMP Documents and Quality Templates!

      Policies & Disclaimers

      • About GMPDocs.com
      • Privacy Policy
      • Terms & Conditions
      • Shipping & Returns

      Subscribe to our newsletter.

      Regular email newsletter about quality assurance and authoring policies and procedures.

      Thank you for your message. It has been sent.
      There was an error trying to send your message. Please try again later.
      payment

      © Copyright 2001 - 2025 | All Rights Reserved

      Page load link
      Go to Top