Following the creation of the final formulation to the satisfaction of the brand owner, the company begins the process of regulatory registration in order to guarantee the product marketing is in accordance with the standards within the destination countries. The process consists of collecting all of the documents required for preparing the Product Information File (PIF), for registering the product in accordance with the requirements of the Ministry of Health and regulatory standards in the destination country, merging all of the information required for preparation of a standards-compliant label for the product, and finally – producing the license. The company, as part of the preparation of the PIF, runs external laboratory tests for all of the product components according to the formula, running a safety assessment and determining which warnings to include in order to ensure safe use of the product.