Discover the usefulness or pharmaceutical quality management systems and the benefits they offer life sciences companies.
Agatha Archives
Meet Agatha at the European TMF summit in London November 14 – 16
f you are headed to the European Trial Master File Summit in London on November 14th – November 16th, then make sure you visit Agatha Inc. booth.
Also, join Ken Lownie’s session as he discusses the evolution of the TMF from file cabinet to process hub.
NS Pharma improves its Quality and eTMF management with Agatha
How Biotech NS Pharma improves its Quality and eTMF management with Agatha. Listen to Arthur Mate, Senior Quality Director explanations.
What is remote monitoring in clinical trials?
Discover the importance of remote monitoring in clinical trials and the best remote monitoring practices.
What is an investigator site file (ISF)?
Discover the importance of investigator site files (ISF) in clinical research and the best methods to keep an organized ISF.
Top 8 eTMF Features
Trial master files are essential for the completion of clinical studies. However, the management of TMF content can be very complex. eTMF systems represent the next step in clinical trial document management and promise to become an integral part of all future...
Agatha Gold partner of the Clinical Quality Oversight Forum on October 24-26, 2022 in Philadelphia, PA
If you are headed to the Clinical Quality Oversight Forum in Philadelphia this October, then make sure you visit Agatha’s booth.
Or better yet, register for Ken Lownie‘s session: What Does a QMS Designed Explicitly for ClinOps Look Like?
Wednesday, October 26 • 11:15am – 11:45am
Benefits of electronic document management in Pharma
Many important processes in the pharmaceutical industry produce a large number of documents. From doctors’ prescriptions to documentation on clinical trials, the amount of information that must be kept on record is staggering. Document-related processes exist on...
5 Steps to Building a Shared Responsibility Model for eTMF
Managing the trial master file (TMF) for a clinical trial is a lot of work. Often, sponsors will delegate TMF management to a contract research organization (CRO). But the truth is, the sponsor can never completely outsource the TMF - ultimately, it is the Sponsor who...
How We Did It: Giving Agatha Apps a Modern User Interface
When you are redesigning an application interface, there are many things you need to think about. It was the same for Agatha’s application interface redesign. In this edition of How We Did It - we’ll take you through the thinking behind the new, modern UI for Agatha...