Our consultancy services

Polymed provides consultancy and project management services for small molecule therapeutics, biologics and medical devices. To discuss your specific requirements, you can contact us on 01451 812 228 or email us at » enquiries@polymed.com

Our expertise covers drug development, strategic reports, regulatory services as well as ad hoc projects including deal making, outsourcing and market and in-licensing assessments. We also have a significant network of scientific experts and opinion leaders.

Drug development

» . Lead candidate selection and optimisation
» . Preclinical programme design and implementation
» . Mechanistic pharmacology
» . Toxicology
» . Safety pharmacology
» . ADME/metabolic studies
» . Reproductive toxicology
» . Clinical trial design and protocol writing
» . Investigator/site selection
» . Clinical trial management Phase I to III

Strategic reports

» . Therapeutic trends and market dynamics
» . Market opportunities for new or re-formulated therapeutics

Regulatory services

» . Europe, North America, South Africa
» . CTA/IND preparation and submission
» . NDA/BLA preparation and submission

Scientific experts and opinion leaders

» . Identification and overview
» . Focus groups
» . Scientific Advisory Boards
» . Non-executive directorships

Other services

Expert Reports, Outsourcing, Quality assurance and compliance, Technical due diligence, In-licensing candidate assessment, Pharma deal making/management, Market research, Medical writing

Access to experts across the spectrum of healthcare

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