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Quality Control Overall product quality of Pharmactive Biotech Products, S.L. is controlled by two departments, the Quality Control Department and the Quality Assurance and Regulatory Affairs Department. The latter is responsible for guaranteeing compliance with external regulations or specific requirements of our customers and ourselves; establishing internal and external mechanisms for the continuous improvement of processes, so as to always ensure the highest quality and safety of our products and services. A perquisite of our quality departments is to provide continuous feedback to all other departments of the company like R & D, Marketing and Sales, etc., as quality is a central theme that runs through a products entire life cycle. From basic research to its final introduction into the market. Quality is also responsible for the integrated management system which we use at Pharmactive, certified according to ISO 9001: 2015 standards on Quality Management and ISO 14001: 2015 on Environmental Management. Likewise, Pharmactive complies with all relevant external regulations on health and safety, both national and international. During 2017, our in-house production facilities have adopted GMP standards and the management system will be certified according to ISO22000. Therefore, our methodology is to introduce quality at the central core of any processes to continually guarantee and improve the quality of any product, and maintain their safety and environmental protection

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