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The effective training of all staff involved in a clinical trial is critical to its success
or failure.
Training is a regulatory requirement and part of your staffs continuing professional
development (CPD).
Rather than delivering theoretical training, CRC specialises in practical training courses
covering real issues that they have encountered in their 25 years involvement with clinical
trials. The course content is specifically tailored to meet the customer’s requirement and
examples of the topics that can be delivered include – good clinical practice (GCP), trial
methodology, pharmacovigilance, the design of SOPs and questionnaire development, regulatory
recommendations, quality assurance, monitoring, data management and data analysis.
To discuss your company's training requirements contact us.
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