Qualification
Safety. Efficacy. Qualtiy.
Qualification and re-qualification are critical in pharmaceutical manufacturing. These intricate, multi-faceted processes systematically evaluate equipment, utilities, facilities, materials and shipping, conducting forensic investigations and media simulations to ensure that each system and product meets the latest regulatory standards of safety, efficacy and quality. Every. Single. Time.
Our strategic planning services ensure that your technology investments support your long-term objectives and provide a competitive edge.
Utilities encompasses the infrastructure of systems and compounds required to run a pharmaceutical production facility, maintaining product quality throughout the manufacturing process. These include thoroughly qualified essential support systems like purified water, compressed air, clean steam, nitrogen, HVAC systems and other critical services that meet strict regulatory standards, influencing the quality of the final pharmaceutical product.
We maticuoulously verify that all working spaces meet pre-determined specifications and regulatory requirements, ensuring that they are suitable for their intended use.
Harnessing our informed expertise, DESA meticulously assesses material suitability to ensure the utmost safety, integrity, efficacy and regulatory compliance.
DESA endeavors to deliver the safest means of transport for pharmaceutical products and medical devices.