Affordable ISO Certification. Ready to use SOPs, Protocols, Master Plans, Manuals and more. In some cases, you may have to scrap defective products and pay additional production costs to replace them. Without them, drug and medical device manufacturing firms will struggle to meet quality standards and maintain their competitive advantage. This can be done through a data reporting procedure used to collect specific data.
We have established a quality policy, objectives, QMS process documents and measures that focus on safety. Each of these innovations was triggered following recognition that a change to the way we do business was required to improve safety. Comor to this postal address Pharmalex Spain. Setting the criteria before initiating the project makes its development much easier. This can help determine if the organization complies with the defined quality system processes and can involve procedural or results-based assessment criteria. Back to the Home Page.