Damien has teamed up with Dr Tony Lockett to deliver a course on the regulations of Phase I/II clinical trials.
The course will be delivered in Leeds on the 25th February 2009.
It is an introductory course on the regulatory aspects of planning a Phase I/II clinical trial, and how these trials should progress the development of your technology. The course is presented by a seasoned professional, who has planed and implemented clinical trials for large pharmaceuticals companies, and small spin out biotechnology companies and national defence organisations, presents a tried and tested course, that will arm anybody planning, running, reporting and purchasing a Phase I/II clinical trial with all they need to know.
For more information on this course or to download the brochure follow this link - Course Details
Damien Bové works as a drug development consultant (pharmaceutical or biotechnology), we work with our clients to define a development target, define a development strategy, define a regulatory strategy or define a commercial strategy. Our clients are generally raising funds or looking to license out their technology and we help them achieve it. If you want to know more don’t hesitate to get in touch using the contact form or email Damien at damien.bove@idaconsultants.com
For Assistance with Regulatory Planning and Exicution of Clinical Trials Click Here
Damien Bové is THE Drug Development and Regulatory Consultant (pharmaceutical or biotechnology), I work with my clients to define a drug development target, define a drug development strategy, define a regulatory strategy or define a commercial strategy. Our clients are generally raising funds or looking to license out their technology and we help them achieve it. If you want to know more don’t hesitate to get in touch.
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