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Submission and Publishing Overview

To complete publication on emc, pharmaceutical companies are required to submit details via the emc Publisher. A valid submission must include a primary document (such as an SmPC or PIL) alongside the associated product.

Publishing Process Overview

All submissions follow a standardised workflow to ensure accuracy, consistency, and compliance:

  • The process begins with the submission of the required document, content, or media link.
  • Content is processed and converted into structured formats (such as XML or HTML) to meet Fast Healthcare Interoperability Resources (FHIR) standards.
  • A Quality Check (QC) is carried out to validate accuracy, completeness, and correct formatting.
  • Following QC, the content may require review and approval by the submitting company.
  • Once all checks and approvals are complete, the content is published on emc.

Recommended Flows

If you are new to emc Publisher, the following workflows are recommended for common tasks:

  • Create a new product using the Create Submission option.
  • Update an existing product using the Create Submission option.
  • Update product details directly via the All Products tab.