The FDA have a technical specification document that describes their requirements for receiving PDF content - https://www.fda.gov/downloads/Drugs/UCM163565.pdf.
At a high level they require that …the PDF generator (ASPOSE) creates PDF files that are readable by Adobe Acrobat X, should not require additional software or plug-ins to be read and navigated. If plug-ins are used during the creation of a PDF document, prior to submitting the document, ensure that a plug-in is not needed for review or archive.
The document also refers to compliance to a series of ISO standards relating to PDF content: PDF (ISO 32000-1), PDF/A-1 (ISO 19005-1:2005) and PDF/A-2 (ISO 19005-2:2011).
Does Aspose have a position on compliance to the FDA requirements document or compliance to the ISO standards: ISO 32000-1, ISO 19005-1:2005 and ISO 19005-2:2011?
Thanks