Detailed definition of a medicinal product, typically for uses other than direct patient care (e.g. regulatory use).

Business idenfifier for this product. Could be an MPID.

Regulatory type, e.g Investigational or Authorized.

The dose form for a single part product, or combined form of a multiple part product.

Whether the Medicinal Product is subject to additional monitoring for regulatory reasons.

Whether the Medicinal Product is subject to special measures for regulatory reasons.

If authorised for use in children.

Indicates if the medicinal product has an orphan designation for the treatment of a rare disease.

Allows the product to be classified by various systems.

Product regulatory authorization.

Package representation for the product.

Pharmaceutical aspects of product.

Clinical particulars, indications etc.

Supporting documentation, typically for regulatory submission.

A master file for to the medicinal product (e.g. Pharmacovigilance System Master File).

The product's name, including full name and possibly coded parts.

The full product name.

Coding words or phrases of the name.

A fragment of a product name.

Idenifying type for this part of the name (e.g. strength part).

Country where the name applies.

Country code for where this name applies.

Jurisdiction code for where this name applies.

Language code for this name.

Reference to another product, e.g. for linking authorised to investigational product.

An operation applied to the product, for manufacturing or adminsitrative purpose.

The type of manufacturing operation.

Regulatory authorization reference number.

Regulatory authorization date.

To indicate if this proces is commercially confidential.

The manufacturer or establishment associated with the process.

A regulator which oversees the operation.