14 Jul 2016 Blog
The 50th Annual Meeting of the DIA 2014

Celebrate the Past and Invent the Future with MaxisIT® at the DIA 50th Annual Meeting, June 15-19 2014 in San Diego, CA!

Hosted this year at the San Diego Convention Center, the DIA Annual Meeting celebrates its 50th anniversary, as a community of life science professionals across all disciplines gather to discuss, share and network with the common goal of fostering innovation in the field of clinical research and development.

MaxisIT® (Booth 2121) will be joining a host of industry experts across all disciplines in the field of life science, with the common goal of coming together and sharing their innovations in pharmaceuticals, biotechnology, medical devices and related medical products.  Please join us at the event to network and share ideas which foster innovation in clinical development with other like-minded professionals.

Team experts from MaxisIT® will be on-hand to showcase how we can help your company leverage information and make decisions in support of clinical research and development.  If you are not familiar with MaxisIT®, we are an Integrated Clinical Development Platform Solution, with the ability to improve how pharmaceutical and life science companies successfully plan, integrate, and accomplish their goals.

Our award-winning CTRenaissance Platform (put link to CTA button here) offers the unique ability to single-handedly manage processes such as study design, metadata repository, programming biometrics, analysis & reporting, drug safety and regulatory standards, modeling/simulation and all steps in between.  However, we do not just offer software as a service.  Our highly qualified outsourcing team experts provide collaborative support to CROs of all sizes, consulting companies, technology providers and clinical operations groups.

We all know clinical trials can be a daunting experience, but with a CTRenaissance Platform and a host of other affordable solutions offered by our Integrated Clinical Development Platform, MaxisIT® can help you successfully leverage all of the necessary steps in one easily maneuverable cloud-based system, saving you both time and money.

Since our inception in 2003, we have earned a reputation as being an invaluable asset in the field, and to us that means we have succeeded in creating a quality system for clinical trial oversight.  Thanks to the DIA 2014 Meeting, we can share it with you in person so you too will be able to see that reputation was justifiably earned.

Be sure to stop by and say hello June 15th through the 19th.  Our MaxisIT® team will be at Booth 2121, and we would be more than happy to speak with you one-on-one about your specific needs.  Feel free to come with questions, as our experts will be able to assist you on the spot.


About MaxisIT:

At MaxisIT, we believe that complex data analysis can produce simple yet powerful insights.

MaxisIT’s Clinical Trial Oversight System (CTOS) is a purpose-built command center designed to manage biopharma and life sciences clinical trials as mission-critical business processes. With its complete AI-enabled analytics platform, the CTOS enables “data-driven digital transformation” from data ingestion, processing, and analysis to in-time clinical intelligence. Its real-time data ingestion, analytics, and visualization empower researchers to identify and address errors as they occur.

The CTOS elevates the value of data, improves efficiency, and empowers clinical stakeholders to seize new opportunities. The platform brings clinical operations and patient data together in a single, central data hub as a single-source-of-truth to help clinical operations, clinical data management, biostatistics, and clinical R&D portfolio management.

A complete self-service, AI-enabled analytics platform, the CTOS unifies trial data from disparate eClinical systems to support study planning, clinical data quality, clinical review, patient safety, clinical operations, CRO performance, risk-assessment, portfolio management, compliance, and submission.

From study setup to data ingestion, clinical trial stakeholders can manage clinical development processes with insight into the study conduct and take proactive actions to reduce costs, mitigate risks, and ensure compliance.

MaxisIT’s CTOS helps you maintain an ongoing health-check on your portfolio of clinical trials, using real-time data, analytics, and visualization to drive rigorous analysis of the entire dataset, allowing for proactive trial risk management.


This website uses cookies to help us give you the best experience when you visit. By using this website you consent to our use of these cookies. For more information on our use of cookies, please review our cookie policy.