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

Doctor Erick

Recent Posts

Life Sciences Job Opportunities in the US

Posted by Doctor Erick on Jul 25, 2017 1:46:21 PM

The Life Sciences sector has evolved over the years, thanks to the burgeoning technological innovation, along with ever increasing patient awareness. Business has been robust for those who are willing to adapt. Despite pricing pressures, economic uncertainty and the general upheaval of an industry in flux, employment prospects for life scientists have remained positive, to say the least. Here are some of the top hiring trends in the bio-pharmaceutical and healthcare industries for 2017:

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Topics: General Medical

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

Clustering Data Streams in Data Analytics!

Posted by Doctor Erick on Jul 17, 2017 4:01:00 PM

The data stream models, with its ability to cater to numerous types of data, have been providing empirical evidence of streaming algorithms based on the performance of synthetic and real data streams. It is crucial to analyze such data provided its ability to process the data in a single pass, or a small number of passes with minimal usage of memory.  Clustering is a key data mining task. This is the problem of partitioning a set of observations into clusters such that the intra-cluster observations are similar and the inter-cluster observations are dissimilar.

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Topics: Data Science

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

5 Must read books on Data Visualization!

Posted by Doctor Erick on Jul 11, 2017 12:46:50 PM

Data Visualization (DV), in simple terms, is the presentation of a data ornate with graphics, which looks aesthetic, when large amounts of data and complex statistics for the easy comprehension. DV is no doubt witnessing exponential growth. No matter whether you are an expert or a novice, a gamut of books are available to hone your skills. If you wonder how you need to know more about DV, all you need to do is to enter the Amazon book section, where you will find in excess of 15,000 items. Let us now see five must-read books on Data Visualization.

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Topics: Data Science

Problems Faced by Foreign Medical Students in the U.S

Posted by Doctor Erick on Jul 6, 2017 2:40:11 PM

There are a plenty of insurmountable challenges that have to be faced by International students who want to get their medical education in the US. Some of the public schools and private universities have very few openings for highly competitive slots for foreign students, adaptability issues and so on. However, it is not impossible though they have to get through several complications in order to gel with the local students and follow their way of an education system. It becomes very challenging for the first time visitors for the reason that the entire atmosphere itself is new and it takes some time to get used to it.

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Topics: General Medical

Migrating CRF to eCRF!

Posted by Doctor Erick on Jun 27, 2017 2:03:33 PM

The necessity to upgrade case report forms (CRFs) happens often during the course of a clinical trial. As a result of advancement in the world of electronic data capture methods, the requirement for Electronic case report forms (eCRFs) has been increased significantly. One should analyze the root cause to such updates in electronic case report forms to acquire efficient knowledge about the migration of case report forms to electronic case report forms. Factors such as protocol amendments, optimized changes made to the eCRF specification requirements and the logic responsible for the automation of the entry or verification of data during the course of study substantiate the needs to migrate to eCRF.

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Topics: Clinical Research

A Risk Management Plan (RMP) For New Applications!

Posted by Doctor Erick on Jun 26, 2017 1:53:31 PM

To describe the safety and efficacy of a medicinal product, a risk management plan (RMP) is inevitable and necessary. In fact, it is the kind of document that describes the current knowledge of the existing trends. The knowledge about the safety and efficacy of the medicine could be gained out of additional activities that are performed in order to fetch key information on plans for studies by the RMP. The risks associated with the use of the product in patients would also be described by a risk management plan with the support of measures to be undertaken to prevent or minimize possible glitches. For any new medicinal product for a human use which must be submitted at the time of application for marketing authorization, the Marketing authorization holders are extremely necessary if they should have an RMP.

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Topics: Drug Safety