This episode offers listeners a chance to become more knowledgeable on how they can audit preparedness, by using internal audits. We will discuss corrective action processes and share strategies for ensuring ongoing quality improvement.

Our goal is to help empower these organization with information on how to maintain compliance and risk management. The ultimate intention is to show how this can ensure that clinical operations stay strong, aligned with the most current cGCP regulations, transparent, and robust.

This episode will use FDA regulations, ICH guidelines, and GMP, quality, and management handbooks to help illuminate this information. We will look at creating a culture that isn't based on cramming, but more of a culture that supports building quality. This helps promote the idea of a culture shift, meaning to create a culture where quality doesn't only come from one department but more of an all-encompassing idea.

This episode serves as a refreshing dive into the key aspects of documentation in clinical trials, making it much more than a dry overview. We'll journey through aspects of informed consent procedures, adverse event reporting, and the very best record-keeping practices.

Ultimately, the intention of this exploration is to provide reliable guidance on how to maintain accurate audit trails. By the end, it will be much more clear that all documentation needs to not only meet regulatory standards but also should support continuous quality improvement.

Throughout the episode, we'll illuminate the crucial role of documentation in all facets of the process. This also incorporates the documentation's role in the ethical process of informed consent, which can give a sense of security to the research.

A look into the key regulations set out in CFR 312.56 illustrates how even sponsors can use record-keeping to monitor investigators and ensure that ethical standards are followed.

This journey into record keeping will not stop at paper records alone. An introduction into the best practices for documenting electronic records will also be examined.

In this episode, we revisit the critical operational components that make up clinical research. This discussion will offer effective methods for monitoring the study process and the key quality assurance procedures that are necessary to support compliance.

We have prepared some practical advice that will give insight into optimizing your processes and will include how to successfully manage risk and prepare for audits. The overall goal is to make these clinical processes as efficient as possible while keeping everything complaint with current good clinical practices.

This information will be delivered by utilizing the heavy hitters of research, for example, Title 21 of the CFR (Code of Federal Regulations). In addition to this, we will also be looking at GMP (Good Manufacturing Practice) and FDA training to deliver this content.

This allows us to emphasize how important it is to have consistent quality in all areas of a clinical trial. We need qualified people running the show and for the research to be completed in a suitable facility.