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

Clinical Research and the impact on humans

Posted by Doctor Dan on Nov 16, 2017 12:59:25 PM

Clinical trials are carefully designed to be as safe as possible for everyone taking part, whichever treatment they receive. Some trials will involve very little risk. In others there may be some side effects from treatments, and finding out more about these side effects is one of the reasons we have trials, says a healthtalk.com report.

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Topics: Clinical Research

Genome Editing Market to reach $5 billion by 2021 from $2 billion in 2016

Posted by Doctor Erick on Nov 6, 2017 12:18:38 PM

The genome editing/engineering market is projected to scale $5 billion by 2021 from the 2016 figure of $2 billion, growing at a compound annual growth rate (CAGR) of 14%, according to a researchnreport.com study report.

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Topics: Clinical Research

Harnessing Technology through Optimization of Patient Engagement

Posted by Doctor Dan on Nov 2, 2017 3:40:46 PM

The combined objective of life science firms and the end-users of healthcare are the enhanced patient outcomes. Often, this has become cumbersome, as the patients find it difficult to browse through the rigmaroles of the healthcare system. For those who live with ailments, the experience can be traumatic, to say the least.

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Topics: Clinical Research

Outcome Health, Harward Health Publications forge alliance to improve digital platforms in clinics

Posted by Doctor Dan on Oct 19, 2017 3:06:21 PM

Fresh off a $500 million first financing round in late May this year, Outcome Health has already set out to improve its health intelligence offerings with the help of a new collaborator: Harvard Health Publications, Angus LLu, Associate Editor, writes on Fiercebiotech.com.

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Topics: Clinical Research

LifeSphere intake and triage to improve efficiency, eliminate manual data

Posted by Phil on Oct 11, 2017 2:51:14 PM

Multi-tenant cloud solution acts as a front end to any safety database and integrates with mobile-based applications to automate and standardize the case intake process for reports received from the field, reducing costs for greater ROI, says an ArisGlobal statement.

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Topics: Clinical Research

eTMFs Are Transforming the Pharmaceutical Industry

Posted by Doctor Dan on Oct 9, 2017 2:50:27 PM

According to a last year’s research on checking the pulse of the pharmaceutical industry’s use of trial master file (TMF) and collating feedback from 217 TMF managers from across the globe shows humongous change is under way as the industry shifts from passive to active TMF management and adopts advanced electronic TMF (eTMF) applications to improve inspection readiness and shorten clinical trial times, Rik van Mol, Vice President of R&D Strategy, Europe, at Veeva Systems, responsible for the Veeva Vault R&D suite of applications writes on pharmexec.com.

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Topics: Clinical Research

Patient Data Access is a Right Guaranteed by HIPAA Regulations

Posted by Doctor Dan on Sep 22, 2017 12:05:12 PM

Individuals have an inherent right to access their own health information. Patient data access can be a critical tool for proper care, but both providers and patients often face confusion about how HIPAA regulations impact the exchange and release of protected health information (PHI).

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Topics: Clinical Research

Environment Monitoring Using Risk Based Approach - 2

Posted by Doctor Dan on Sep 19, 2017 12:58:22 PM

In the Clinical Research arena, the Environmental Monitoring (EM) Program - comprising of viable and non-viable monitoring elements – is designed to routinely monitor particulates as well as micro-organisms in key spears of pharmaceutical manufacturing facility, especially in the aseptic processing areas. While the viable or micro-biological monitoring is replete with routine monitoring of the manufacturing environment for the trace of micro-organisms, the non-viable particulate monitoring, calculates the airborne particle count and further offers inputs on the routine maintenance of the clean room air classification.

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Topics: Clinical Research

Amazon might foray into Clinical Trials Segment

Posted by Doctor Dan on Sep 18, 2017 12:43:12 PM

The global e-commerce Major Amazon has made many awestruck with its foray into the hitherto untapped area of healthcare. Although, the company has a perfect platform for selling any product under the sun, including pharmaceutical items, but then why should it get into healthcare segment is the question that begs an answer, according to medium.com report.

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Topics: Clinical Research

Mobile Data For Clinical Trial-2

Posted by Phil on Sep 15, 2017 4:22:53 PM

A new research report, published in the Journal of Medical Internet Research reveals that the mobile device (Mobile Technology) can effectively support a slew of things within the clinical research such as project management, data management, and telemonitoring, according to a mhealthintelligence.com report.

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Topics: Clinical Research