Examples of 'marketing authorization' in a sentence
Meaning of "marketing authorization"
Marketing authorization is the official approval granted by regulatory authorities for the marketing and sale of a pharmaceutical product. It confirms that the product has undergone rigorous testing and has met the required quality, safety, and efficacy standards. Obtaining marketing authorization is a crucial step in the process of bringing a new drug to the market
How to use "marketing authorization" in a sentence
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marketing authorization
Third countries in which a marketing authorization is granted.
The marketing authorization holder shall.
Name and address of marketing authorization holder.
Marketing authorization process is ongoing.
Specifications are in compliance with the marketing authorization.
Filings for marketing authorization for new products.
The specification contained in the marketing authorization or.
Application for marketing authorization for veterinary medicinal products.
Variation to the terms of a marketing authorization.
The absence of a marketing authorization is a risk to health and safety.
Procedures relevant to the marketing authorization.
Marketing authorization holder.
Two drugs obtained a marketing authorization.
Marketing authorization applications for this indication are in progress in several countries.
Annex iv conditions of the marketing authorization.
See also
marketing authorisation valid
marketing authorisations
marketing authorizations
marketing automation
marketing authorisations
marketing authorizations
marketing automation
Rules relating to marketing authorization of medicinal products for human use.
Name and permanent address of holder of the marketing authorization.
A basic directive relating to marketing authorization of veterinary medicinal products.
Mentions that the medicinal product has been granted a marketing authorization.
Procedure for marketing authorization.
Manufacturers of generic drugs refer to this data regularly to obtain marketing authorization.
Variation to the marketing authorization.
In the marketing authorization should be carried out according to the approved methods.
Anyone wanting to manufacture a drug must get a marketing authorization to do so.
Constitution of the marketing authorization application dossiers for biocidal products.
Name or corporate name and permanent address of the marketing authorization holder.
Notice to applicants for marketing authorization for a proprietary medicinal product.
Transitional measures for any implementation of the new marketing authorization procedures.
The absence of a valid marketing authorization is considered a risk to health and safety.
Explanation of its significance at a later date are part of the conditions of marketing authorization.
The reasons for the refusal of a marketing authorization shall be given.
Detailed assessment report with comprehensive overview of reasons for refusal of marketing authorization.
Each drug must have a marketing authorization for each indication.
Before vending any medical product must have passed marketing authorization.
The references of the marketing authorization and of the patent concerned shall be given.
These conclusions are mainly in line with studies conducted post marketing authorization.
Instance a complete application for marketing authorization should be submitted to the competent authorities of the.
Opinion of the committee for proprietary medicinal products on the granting of a marketing authorization for.
Eec directives relating to the marketing authorization for medicinal products for human use.
Medicated feed may be prepared only from medicated premix that has been granted marketing authorization.
The marketing authorization holder assumes no liability for damage resulting from unintended use.
Transparency of the documents submitted in the context of a marketing authorization application for a medicinal product.
A marketing authorization may only be granted to an applicant established in the Community.
They should comply with the relevant parts of the manufacturing and marketing authorization dossiers.
The system of marketing authorization provided for in that Directive.
Most countries have a regulatory authority and formal requirements for providing marketing authorization for medicines.
The marketing authorization of VMP does not require the payment of any fees.
The central government is responsible for the marketing authorization for GMOs and products containing GMOs.
Medicinal products for human and veterinary use subject to the centralized procedure for marketing authorization.
Steps taken after granting the marketing authorization No links.
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