With 30 years of experience in clinical trials and regulatory affairs, Dr Phillip Altman, BPharm(Hons) PhD is a Life member of ARCS and is well known to the pharmaceutical, medical device and biotech industries.  His wide range of skills are particularly useful to start-up companies requireing expert broad ranging advice, planning and budgeting where senior level consulting is required.  Dr Altman networks to specialist experts around Australia wherever appropriate.

• protocol drafing and CRF design
• ethics committe applications
• total clinical trial management
• monitoring
• data management
• report writing
• project management; feasibility
• product development advice
• member of Scientific Advisory Boards

Regulatory Affairs; Medical Writing; Clinical Research; Data Management