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"Our research and development experience provides a context that goes hand in hand with our other training experience and allows us to build on an extensive knowledge base. It fits naturally with our core competencies."
Paul LaFerriere
Chairman of the Board, Founding Partner
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| CLD has experience describing the drug discovery process for audiences such as newly hired research scientists, global marketing personnel, legal/regulatory personnel, and sales personnel.
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| CLD has developed White papers and workshops as well as online materials for research scientists relating to pre-clinical and clinical issues such as dose selection, hepatotoxicity, drug interactions, and QT prolongation. Documentation of data management processes for development of drug databases has also been a topic.
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| CLD has developed a training workshop for new investigators about protocol development and clinical trial milestones to train potential new investigators in the topics needed to perform clinical trials that meet ICH requirements.
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| CLD has written and trained pharmaceutical personnel on SOPs for clinical research associates as they relate to the conduct and reporting of data.
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| CLD has developed modules, videos, ancillary materials, case studies, and scenarios all relating to the legal and regulatory requirement of the safety reporting process. These materials are also available in an online format.
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