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COUNCIL DIRECTIVE of 17 March 1997 amending and updating Directive 64/432/EEC on health problems affecting intraCommunity trade in bovine animals and swine 97/12/EC (OJ No L 109, 25.4.97,.p 1) amended
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Council directive 97/12/EC is a European Union directive that establishes procedures for the marketing of medicinal products for human use.
Pharmaceutical companies and manufacturers are required to file council directive 97/12/EC.
Council directive 97/12/EC must be filled out by providing detailed information about the medicinal product, including its composition, manufacturing process, and labeling.
The purpose of council directive 97/12/EC is to ensure the quality, safety, and efficacy of medicinal products for human use.
Information such as product composition, manufacturing details, labeling information, and product registration details must be reported on council directive 97/12/EC.
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