A campaign to encourage the public to think differently about clinical research has been a top initiative at the Center for Information and Study on Clinical Research Participation (CISCRP).
Dr Phil Hewitt, talks to NGP’s Rebecca Goozee about the challenges and developments of toxicogenomics at Merck KGaA.
A great drug, a well designed protocol, excellent monitoring, and stringent human subject protection measures account the majority of what is needed for a successful clinical trial.