NextPharma is a business operating as a strategic outsourcing partner to the pharmaceutical industry for pharmaceutical development, commercial manufacturing of medicinal products (including the manufacture of investigational medicinal products for clinical trials), contract packaging and logistics services.
It is the policy of NextPharma to ensure that all products and services offered to our company's customers consistently conform to all applicable regulatory requirements and with the principles and guidelines of current Good Manufacturing Practice (cGMP) to ensure a "fitness for use" expected by our customers' contractual expectations.
Furthermore, it is our policy to ensure that (1) NextPharma’s facilities and (2) product development, manufacturing and logistics processes that directly affect the quality of the final medicinal product, are identified and controlled to provide a high degree of assurance that each commercial product consistently meets its pre-defined specifications and quality attributes.
NextPharma conducts its business in accordance with the relevant global regulatory requirements, including European Directives 2001/83/EC and 2003/94/EC, code of federal regulations parts 210 and 211 and other global territory regulatory guidance.
Read more about our Quality Mission Statement.
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