ISA 230 is the overarching documentation standard and it applies to all audits of financial statements.
It contains general audit documentation requirements and, among other matters, covers the form, content and extent of audit documentation and the assembly of the final audit file.,Audit documentation should be prepared in sufficient detail to provide a clear understanding of its purpose, source, and the conclusions reached.
Also, the documentation should be appropriately organized to provide a clear link to the significant findings or issues.,Audit documentation should be prepared in sufficient detail to provide a clear understanding of its purpose, source, and the conclusions reached.
Also, the ,Demonstrate that the engagement complied with the standards of the PCAOB,Support the basis for the auditor's conclusions concerning every relevant financial ,Effective Date of Standard: For audits of financial statements, which may include an audit of internal control over financial reporting, with respect to fiscal
\nGood documentation practice is a term in the pharmaceutical and medical device industries to describe standards by which documents are created and maintained.While some GDP / GDocP standards are codified by various competent authorities
Others are not but are considered cGMP.Some competent authorities release or adopt guidelines
And they may include
Non-codified GDP / GDocP expectations.While not law
Authorities will inspect against these guidelines and cGMP expectations in addition to the legal requirements and make comments or observations if departures are seen. \nIn the past years
The application of GDocP is also expanding to cosmetic industry
Excipient and ingredient manufacturers.
Explicit implementation of requirements to be satisfied by a material, design, product, or service
\nA specification often refers to a set of documented requirements to be satisfied by a material
- Design
- Product
Or service.A specification is often a type of technical standard.