Pharmaceutical Development Services Limited is a pharmaceutical consultancy assisting clients with regulatory, quality and manufacturing services in Europe for pharmaceutical products and medical devices. We specialise in assisting US companies perform clinical trials and market products in Europe and offer a turnkey operation if required. PDS was formed in 2000 and has an extensive network of consultants who provide detailed and up to date specialist technical knowledge. PDS consultants also work as experienced interim managers for senior positions in Regulatory Affairs, Pharmaceutical Development and Quality Assurance. PDS works with a range of clients from small start- up biotechnology companies to large multi-national pharmaceutical companies. Contractor Management: PDS consultants assist companies in the placing of work with CROs from the preclinical stage to Phase 3. Technical Development: PDS advises companies on the strategy for introducing a new product, from pre-clinical technical development to a multi-national commercial launch. Regulatory Affairs: PDS provides strategic regulatory advice and support for agency submissions, due diligence and writing regulatory dossiers. From small molecules to botechnology compounds, PDS has expertise with herbal medicines, nutraceuticals, cosmetics and medical devices. Training: We provide expert in-house and public training courses through our sister business PharmaTraining Services (www.pharma-training-courses.com).