Marketing & Advertising - Flemington, New Jersey, United States
Robert Krell creates readable, patient-friendly, visually enhanced informed consent documents and clinical trial materials for study sponsors. Krell has focused on improving informed consent forms (ICFs) by correcting the problems of readability and comprehension.Krell's proven solution for better informed consent are visually enhanced informed consent documents written in plain language at or below 8th grade reading levels, which meet or exceed the recommendations and requirements of US and global regulatory authorities, local and central IRBs, as well as the International Conference on Harmonisation guidelines.Krell offers specialized communications expertise in drug development and clinical trials for CROs, pharmaceutical, biotechnology, and medical device companies. Krell has extensive knowledge of all phases of drug development, outsourcing, specialized clinical trial services and the various roles and sensitive relationships between sponsors, clinical trial teams, IRBs, investigators, legal and regulatory reviewers, and other stakeholders.For more information about informed consent documents, study brochures , patient recruitment, study websites, and study branding, contact Robert Krell at robertkrell@mac.com