About Sollers

Sollers is a graduate school located in New Jersey, specializing in clinical research, drug safety and pharmacovigilance training.

Our graduate certificate and masters programs cover a wide range of subjects tailored to this fast growing industry, and our graduates go on to highly successful careers in the pharmaceuticals industry and healthcare industries.

  • HOURS
  • Monday - Thursday | 10 AM - 7 PM
  • Friday | 12 PM - Midnight
  • Saturday | 12 PM - Midnight
  • Sunday | Closed
  • OPEN 24/7 - sollers.edu
    • PHONE
    • (848) 299-5900
    • Location
    • 100 Menlo Park, Suite 550
      Edison New Jersey 08837 -2488

Location

Call Us Now: 848 299-5900

Sollers Blog

Benefits of Data-Management Plan!

Posted by Doctor Erick on Jul 31, 2017 4:12:55 PM

Data-Management Plan (DMP) is a formal document describing how you plan to handle research project data during the research and after the research is completed. It describes what tools & techniques you will use to collect, store, manage and analyze this data. Mechanism to preserve research data and means to share it with others also form a part of DMP. Most agencies, which fund the research projects, require a DMP with every funding request.

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Topics: Clinical Research

Risk Based Monitoring!

Posted by Phil on Jul 27, 2017 2:19:34 PM

Join the Program on Risk Based Monitoring (RBM)  

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Topics: Clinical Research

Opportunities for a Data Clinical Manager

Posted by Doctor Erick on Jul 27, 2017 1:43:43 PM

Clinical Data Management or CDM is an important area of clinical research and studies. Healthcare organizations and hospitals employ Clinical Data Managers for their organizations.

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Topics: Clinical Research

Environmental Monitoring using Risk Based Approach

Posted by Doctor Dan on Jul 24, 2017 2:27:50 PM

In order to routinely monitor particulates and micro-organisms in critical areas of a pharmaceutical manufacturing plant, more particularly in the aseptic processing areas, the environmental monitoring (EM) program has been designed, which comprises of viable and non-viable monitoring elements.

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Topics: Clinical Research

Mobile Data Capture in Clinical Trials: An Overview

Posted by Doctor Dan on Jul 21, 2017 3:43:22 PM

The introduction of mobile device-based electronic data capture system (mEDC) technology is indeed a boon for clinical trials, as per a research report. According to the new research paper published by the Journal of Medical Internet Research, the mobile device is of immense help in terms of supporting a slew of services within clinical trials such as project management, tele-monitoring, and data management, among others.

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Topics: Clinical Research

6 Healthcare Revenue Cycle Management Systems to Watch!

Posted by Doctor Erick on Jul 18, 2017 12:35:05 PM

Healthcare organizations and hospitals are engaged in providing the healthcare services all the time. These services are crucial for treating, monitoring and assisting patient well-being.  They take care of patient requirements from admitting, treating, scheduling appointments and providing specialized services.

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Topics: Clinical Research

Risk Based Monitoring Workshop by Dr. Nimita Limaye!

Posted by Doctor Dan on Jul 14, 2017 11:50:29 AM

Join us for an in-depth session on Risk Based Monitoring Workshop by Dr. Nimita Limaye!

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Topics: Clinical Research

Risk Based Decision Making - An overview

Posted by Doctor Erick on Jul 13, 2017 1:41:16 PM

Drug safety industry is on the verge of comprehensive analysis phase to determine the possible conditions and process involved in risk-based decision making. Pharma industries take a leap to advanced mechanisms that are systematically approved for implementation. It can be assessed based on its post-marketing strategies which are completely based on regulatory decisions. Improved information statistics to the risk-based decisions appear to be ad hoc, informal and qualitative. The more systematic and scientific behavior is risk-based assessment that could be used for the employment of thorough drug safety efficacies. Possible recommendations of assessments in the drug safety industry include the corresponding behaviour analysis of drugs directed towards the FDA in the preapproval and postapproval settings.

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Topics: Clinical Research

What is Openclinica?

Posted by Doctor Dan on Jul 13, 2017 12:57:30 PM

Openclinica has been known as the world’s first commercial open source clinical trial software serving for the purpose of clinical data management (CDM) and electronic data capture (EDC). Openclinicia is immersed in clinical trials and different types of clinical research areas.

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Topics: Clinical Research

End to End Patient Engagement in Clinical Research!

Posted by Doctor Dan on Jul 7, 2017 11:16:34 AM

Complete involvement of patients in their personal healthcare is known as End-to-End Patient Engagement. In today's world, this is primarily accomplished electronically through Patient Engagement Technology that involves hardware, software, and services. This technology is an important tool for clinical research and trials.

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Topics: Clinical Research