Pharmaceutical Solutions offers a range of Qualified Person and Quality Assurance services to the pharmaceutical industry.
Pharmaceutical Solutions holds a Manufacturer’s Authorisation (IMP12623/00001) to certify batches of Human Investigational Medicinal Products for EU clinical trials. We are licensed to certify or import and certify sterile, non-sterile, and biological investigational products.
With Manufacturer’s Authorisation MIA(IMP) 29826, Pharmaceutical Solutions can certify batches of Human Investigational Medicinal Products for clinical trials in Great Britain. We handle sterile, non-sterile, and biological investigational products and import intermediates for further processing.
Licensed to import QP certified investigational medicinal products from approved countries into Great Britain, Pharmaceutical Solutions oversees the entire importation process, covering all dosage forms.
Pharmaceutical Solutions staff are Qualified Persons under Directive 2001/83EC, working on Marketing Authorisations in Great Britain for various dosage forms, including sterile and non-sterile products, biological products, medicinal gases and veterinary products.
Pharmaceutical Solutions offers comprehensive audit programmes and one-off audits to various standards, including EU GMP, cGMP, GDP, and ISO standards. We perform audits independently or as part of a customer team, in an open and consultative manner, ensuring thorough assessments and comprehensive reports.
We provide Quality Assurance and Quality Management System assistance, including developing and implementing quality systems, conducting gap analyses, training, inspection readiness preparation, post-inspection improvement, and emergency QA cover.
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đź“ž +44 (0) 1829 749021
đź“Ś The Old Bakery, High Street,
Tarvin, Cheshire, CH3 8JA, UK
đź“Ś 51 Bracken Road, Sandyford,
Dublin, D18 CV48, Ireland
📧 info@qpservice.co.uk
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