This SOP establishes procedures for the approval or rejection of product batches manufactured or retail packaged.
This SOP, report and report log establishes procedures and provides resources to document and investigate calibration failures as required by 21 CFR 111.
This SOP, report and report log establish procedures and documentation for deviations from instructions provided in the Master Manufacturing Record, standard operating procedures, or other specification documents, with the deviations being temporary and approved in advance by quality assurance (QA) and other management
This SOP, report template and log establishes procedures and documentation for corrective and preventive actions that are NOT related to specific lot(s) or batch(es) of production material.
This SOP establishes procedures for documenting and investigating production failures. An investigation production failure report template and report log are also provided.
This SOP establishes procedures for documenting unexpected occurrences and unplanned deviations from the instructions provided in the Master Manufacturing Record, standard operating procedures, or other specification documents. An unplanned deviations report and report log are also provided.
2021 Annual Fund Sponsors
AHPA appreciates the support of its sponsors, but does not endorse, recommend, or provide a warranty for any sponsor company, its products or services. AHPA has no responsibility for any transaction entered into with any of these companies.