Quality without compromise
Quality Assurance covers every aspect of the way we work to ensure that quality is maintained throughout the whole process.
Our commitment to meeting the requirements of ISO 9001:2008 and ISO 13485 (Medical Devices) as well as Good Distribution Practice (GDP) and Good Manufacturing Practise (GMP) enables us to ensure quality from receipt of initial enquiries through to delivery of the consignment.
Manufacturing is a collaborative process between like-minded scientists who refuse to compromise on standards. We’ve formed a number of strategic alliances with manufacturers who share our commitment to excellence and to international quality standards.
Manufacturing facilities undergo a thorough selection process and as a result all products are manufactured in up-to-date facilities. In addition, we review individual product documentation and undertake site audits. Our quality management programme demands continual assessment of our supply chain.
We have procedures in place to efficiently and effectively manage medical enquiries, adverse events and quality complaints, as well as full batch traceability.
Medicines supplied by Morningside Pharmaceuticals meet appropriate international standards of healthcare. Products comply with British, European or US Pharmacopoeias (where applicable) and manufacturing facilities meet GMP as specified to WHO (World Health Organisation) or European Union (EU) standards, as appropriate.
Medical Devices for International markets
Our Sensecure® and Medifend® ranges hold CE marking where appropriate and are manufactured in accordance with EU Medical Device Directive 93/42/EEC as amended by 2007/47/EC. Morningside Pharmaceuticals maintains ISO 9001:2008 and ISO 13485:2003 through British Standards Institute (BSI), UK.