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

Outcome-Based Contracting Means for Drug Development and Pricing

Posted by Doctor Dan on Jul 25, 2017 2:44:18 PM

The pharmaceutical industry is facing intense pressure to lower drug prices and curtail the price increase in the recent years. This has been due to a dramatic increase in the cost for some high-profile and certain life-saving drugs. The high cost of drugs makes it difficult for patients who are in need of medicines on the regular basis. The increasing cost is a source of stress to the patient and his family.

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Topics: Drug Safety

What are Psychedelic Drugs?

Posted by Doctor Dan on Jul 20, 2017 3:28:27 PM

Psychedelic DrugsPsychedelic drugs are substances whose primary aim is to change the cognition and perception of people who take them. They are also called as psychotomimetic drugs. They form part of a group of drugs called hallucinogens which also include dissociative and deliriants.

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Topics: Drug Safety

Opportunities for a Drug Safety Specialist!

Posted by Doctor Dan on Jul 17, 2017 12:58:09 PM

The scope for drug safety specialists is manifold. Given the space for new candidates who take-up drug safety specialist as their career the opportunities have been widely sought-out in the industry. There are plenty of drug safety jobs such that over 2,000 professionals every year are recruited for leading pharmacovigilance positions throughout the medical industry, in settings including clinical research organizations, the NHS, biotechnology firms and pharmaceuticals companies. The people working in the drug safety industry are extremely responsible for monitoring the safety of the products, interwoven with duties including detecting, assessing and preventing adverse events considering that pharmacovigilance is an extremely important element of the development, trials, marketing and continued use of any medication.

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Topics: Drug Safety

Economic Impact on Drug Safety and Pharmacovigilance

Posted by Phil on Jul 12, 2017 3:46:28 PM

Drugs can enter the market only when these are found safe for use. Pharmacovigilance and safety of any drug is crucial to any clinical research.  It includes many aspects of well-being of the patient, trust, and confidence in the pharmaceutical industry and the field of medicine. Another important facet is the economic impact of drugs and drug safety issues.

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Topics: Drug Safety

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

Insights about 'Alliance for Safe Online Pharmacies'  (ASOP)

Posted by Doctor Dan on Jun 22, 2017 12:36:34 PM

The ASOP Global is dedicated to helping consumers stay safe online among more than 33,000 illegal online pharmacies. The LegitScript URL verification tool or search the National Association of Boards of Pharmacy’s database of verified pharmacy websites shall be used to ensure the online pharmacy sites you visit are safe and legitimate. Of late, the 'Alliance for Safe Online Pharmacies' tied-up with new partners such as the International Alliance for Patients' Organizations (IAPO), Consumer Online Foundation (COF) India, National Council on Patient Information and Education (NCPIE), and Healthcare Distribution Alliance (HDA). There are around 276 member organizations from 71 countries representing 50 disease areas under the International Alliance for Patients' Organizations (IAPO) and it is regarded as one of the hosts of the March 2017 International Forum on Patient Safety and Access to Safe Online Pharmacies in New Delhi, India, an event organized by ASOP Global.

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Topics: Drug Safety

Required Time for a Pharmacovigilance Audit

Posted by Doctor Dan on Jun 20, 2017 11:00:16 AM

The expertise and its tools to assist in the identification of the processes to be covered, as relevant to the sites audited will be compiled and presented by pharmacovigilance audit. Some of the processes to be carried during a pharmacovigilance audit are maintaining Core Safety Information, ensuring Periodic Safety Reporting (PSUR, DSUR...), to involve in a possible, Interaction between Drug Safety and Technical Quality Assurance Organization (Quality Complaints), roll out Literature Screening, assessing relevant Responsibilities and Organization for Pharmacovigilance, to interact between Drug Safety and the Medical Information Organization (Medical Enquiries), managing safety-related Processes in Clinical Trials, to process and submit the possible results of Individual Cases, performing Signal Detection and management, overseeing Risk Management including pharmacovigilance planning, to take privilege in the Maintenance of approved Product Information and Validation of Computer Systems, Security, Back-up and Disaster Recovery, to formulate training and Quality Management Systems.

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Topics: Drug Safety

Drug Safety Market - An Overview!

Posted by Phil on Jun 14, 2017 1:29:38 PM

Drugs are administered to patients to make them well, ease disease and prevent complications in chronic conditions. However, drugs need to be prescribed, administered and meticulously monitored to safeguard the health and life of patients.

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Topics: Drug Safety

Job opportunities for a Drug Safety Associate!

Posted by Phil on Jun 12, 2017 2:31:53 PM

When new drugs enter the market, they need to be tested for safety. It has to be declared safe and competent and not just restricted to clinical trialsIn spite of FDA regulations and guidelines for the drug to be marketing the pharmacovigilance team needs to supervise and monitor the drug to label it safe for consumption to enhance better health.  This pharmacovigilance or drug safety requires trained manpower to study the drugs and their safety. Drug safety associate studies the drug, its effects and depending upon the analysis, terms it safe or unsafe for patients.

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Topics: Drug Safety

Future of bio-manufacturing

Posted by Doctor Dan on Jun 6, 2017 12:13:06 PM

The future of biomanufacturing is highly dependent on the current trends of pharmaceutical industry where a number of innovations have flourished over the recent few years. Beginning from a small-molecule success ratio, the pharmaceutical manufacturing has seen its highs and lows with the discovery of a vast variety of drugs and new facilities. Even though the industry is in the successful era of its development, there are still a wide number of factors in the biopharmaceutical manufacturing that still remain untouched by the challenges facing the industry as a whole. Before delving into prospects of bio-manufacturing, a sneak peak of current treatment employed in manufacturing industries is very necessary. As of today's trend whether it is the manufacturing of hormones, recombinant proteins or monoclonal antibodies, the drug makers have developed a habit of setting up biological factories.

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Topics: Drug Safety