This in-depth training course presents a thorough overview of the fundamentals of technology transfer, providing a practical guide to overcoming the challenges you will undoubtedly face on a daily basis. Our dedicated instructors will ensure all participants are able to manage project development issues effectively and feel completely at ease with the theory behind technology transfer. An examination of the key regulations and guidances will be followed with a review of the crucial elements needed to guarantee compliant record keeping practices are in place.

Who Will Attend?
This course is highly recommended to anyone working in pharmaceutical, medical device, biotechnology or biologics companies in the following departments:
> Product Development
> Chemical Development
> Manufacturing & Production
> Quality Assurance
> Project Management
> Engineering

Course Leader
Dr Trevor Deeks Manager of Validation and Regulatory Compliance, Europe, Fluor Daniel – 22 years experience in pharmaceutical manufacturing, development, quality assurance and validation, including several years in senior management roles with major pharmaceutical manufacturing companies and more recently with contract validation and consulting groups. Qualified Person under EC legislation and a registered pharmacist. Managed a number of large validation projects, performed many audits and mock inspections and acted as an auditor for both the WHO and UNICEF. Over 30 papers published in peer reviewed journals, contributions to a number of books including the Pharmaceutical Codex.