What is readability, and why should the research community be concerned about it? Readability refers to the ease of reading and understanding written information. At this time and for the…
The DHHS issued a News Release in July regarding proposed changes to the “Common Rule”, and is welcoming all comments regarding changes that would affect biomedical and social/behavioral research. Highlights…
A clinical trial is only as good as the records kept by investigators and their research teams. Research sponsors tend to be very specific in outlining their expectations for records…
The U.S. Department of Health and Human Subjects (HHS) recently issued a press release outlining proposed changes to the “Common Rule”, which has gone essentially unrevised since its adoption in…
Enclosure cards are used to identify the enclosure inhabitants, as well as any other pertinent information regarding their numbers, gender, care, or anything else that may be important to their…
The memberships of institutional review boards for Human, Animal, and Safety committees are defined by federal and state regulations. In general, each committee must have a Chair, scientific/physician members, non-scientific…
InfoEd’s Animal Facilities Management module can help track the health status of your animals! An integral component of tracking animals throughout an approval period of a protocol is the maintenance…
The Clinical Trials module (CT) provides two options for setting up a detailed clinical trial plan, which in InfoEd’s terminology is called the Procedure Matrix. Clients not using the Financials…
The Animal Facilities Management module is used to operate an animal facility and track animal inventory. In addition to tracking individual animal information, facility administrative staff can use the Census…
The Environmental Health and Safety Management module provides the capacity to track and report on the staff and user certifications to handle and use hazardous substances, including radioisotopes, harmful chemicals,…