Quality control & manufacturing quality
Here at H&T Presspart, we have a long term commitment to quality and testing.
We will never compromise our high standards, and perfection and precision have remained our top priorities over the decades.
We understand fully that quality control and stringent testing are more important in the pharmaceutical industry than in any other. Regular audits by some of the World’s leading pharmaceutical names ensure product compliance to the highest functional and regulatory standards.
Our systems and facilities comply with ISO 9001, ISO 14001 and EU/FDA Good Manufacturing Practices (cGMP) ensure the highest standards are adopted across the business. Packaging and coating of pharmaceutical products is carried out within a clean room environment to ensure the lowest possible risk of contamination.
Our in-house analytical laboratory services, and state-of-the-art testing and measuring equipment, along with our quality record – demonstrate a continuing company commitment to satisfying customers’ needs. It is due to our exacting standards and insistence upon superior service, that long-term customer partnerships have become ‘the norm’ at H&T Presspart.
Whether you need a technology or manufacturing transfer, or a conceptual design taken through to a commercial solution, the pharmaceutical team at H&T Presspart can deliver successful results.
Specifications, design, management, installation, validation, maintenance and continuous improvement of equipment and manufacturing processes are all carried out to the highest pharmaceutical regulatory compliance and standards. They are also clearly illustrate a strong project managerial pedigree.
H&T Presspart’s process engineering toolbox, from Six Sigma, Lean Sigma and Kepner-Tregor further enhance project management capabilities. FMEAs, Process Mapping and data-driven analysis ensure a philosophy of continuous improvement across the business.