Stuart Reed Email & Phone Number

Epsom, Gb

United Kingdom

An independent consultancy specialising in high quality ad hoc resource to manage our clients need for flexible peak resource.

London, England, United Kingdom

Phuturum believes that every pharmaceutical company can unlock its full regulatory affairs execution potential. Powered by its data and submission and knowledge core platform, we provide a means to automate non-complex data driven regulatory activities, eliminating millions in regulatory inefficiencies, compliance burdens and personnel costs and driving critical medicines and healthcare to patients 10x faster.

Surrey

Independent Consultant to the Pharmaceutical Industry, specialising in Regulatory Affairs strategy and Outsourcing projects

Contract placement with Pharmalink Consulting, working on product maintenance of Centralised and MRP products within the Shire Portfolio.

Working on a number of contract placements within client companies on all aspects of Regulatory Affairs including Prescription, OTC and cosmetic registrations, Regulatory submissions and maintenance for centralised, mutual recognition and national registrations, clinical trial applications, regulatory strategy and regulatory intelligence.

Contract Placement: Project Manager for Global Site Transfers in all regions except US and Canada. Part of a Company initiative to rationalise manufacturing for all its products. Managed a small team of junior personnel ensuring project timelines and targets were met.

Contract Placement: Worked with the Anti-Infectives and Anti-Inflammatory therapeutic group on regulatory strategy, product maintenance and CTD work

Contract Placement: Smoking Cessation and Oral Health Care (cosmetic) European Regulatory lead. Post Marketing Regulatory Maintenance, Regulatory Strategy and product development, SPC and labelling changes, dossier preparation and submission coordination.

Contract Placement: European Clinical Trial Applications, UK CTX's, Expert Reports (CMC, Tox and Clinical)

Contract Placement: NTA Part I, Part II and Part IV work. Company was bought by ICON Clinical Research during contract placement here.

Contract Placement: Safety and labelling group, SPC changes worldwide.

Contract Placement: Labelling changes, dossier consolidation and preparation,

Part I, II, III and IV work, Centralised application (pre-submission), dossier compilations, SPC preparations, ghost writing of Expert Reports.

Secondment to Novartis Consumer Healthcare, Switzerland. Acted as Regulatory Liasion for European affiliates while position was advertised for replacement. Answered regulatory queries, caretaker of Regulatory Category Manager role for Digestive Health, Neutraceutical and Topical Health Care categories.