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Handy Consulting Ltd was established, and is led, by Louise Handy, an experienced consultant in quality assurance, regulatory affairs and strategic management

Director

Louise’s background is in scientific research, originally qualifying as an immunologist. She undertook a wide range of research in hospital & academic laboratories before being instrumental in establishing a new accredited pathology laboratory to service the clinical trials industry.

Subsequently she became CEO of a successful independent phase 1 clinical trials unit and has held other senior management positions and Directorships in publicly and privately funded pharmaceutical & healthcare related organisations. As a result she has comprehensive experience throughout the length of the pharmaceutical and scientific research & development process.

Having provided quality, regulatory & business advice & training for many years, she has been teaching & consulting as an independent professional since 2004.

• Director, Chair Elect and Fellow of BARQA
• Institute of Clinical Research Professional Member
• Chartered Management Institute Member
• Thorough knowledge of GCP, GCLP, GPvP, GMP, GDP, GLP  & ISO requirements & systems, invaluable for implementation and auditing.
• Author of Quality Systems Workbook
• Leading role in developing internationally recognised Quality Guidelines for non-regulated scientific research (Good Research Practice)
• Experienced professional development course & MSc module developer and tutor
• QP for Pharmacovigilance
• Reputation for successful strategic planning and implementation - qualified in Strategic Management
• Speaker at international conferences
• Has lead computer systems validation (e.g. LIMS and stock control)