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

Bio-Pharma Packaging Industry: An Overview

Posted by Doctor Dan on Aug 4, 2017 11:07:10 AM

Global pharmaceutical packaging market is projected to touch $104,882 million by 2022 from $68,749 million in 2015, growing at a CAGR of 6.27% from 2016 to 2022. With humongous investments in Research and Development, innovations in packing materials, burgeoning growth in generic market and heightened trend of contract packaging will spur the growth in this segment in the coming years.

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Topics: Drug Safety

Supplier Relationship Management

Posted by Doctor Erick on Aug 2, 2017 11:39:09 AM

It was the period when McKinsey consultant Peter Kraljic defined corporate buyers to grow more proactive in supply management that Supplier Relationship Management (or SRM) came into life in the year 1983. Since then it has been a great source for the development of various sectors such as Supplier Relationship, Drug Safety and Electronic Data Capture (EDC) Clinical Data Management (CDM).

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Topics: Drug Safety

Virtual Pharmaceutical Companies: A Synopsis

Posted by Doctor Dan on Jul 31, 2017 1:48:14 PM

The virtual entities have become significant in the pharmaceutical industry. Apart from selling major brands of drugs online, these firms are also aiming at making own products. Although some virtual companies may aspire to become full-fledged manufacturing companies one day, many do not, but focus on milestones and licensing deals. Vertex Pharma is a classic instance of a virtual pharmaceutical company that thrives on the online space.

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Topics: Drug Safety

Why choosing Drug Safety Course is a better option?

Posted by Doctor Dan on Jul 28, 2017 2:38:03 PM

Choosing a Drug Safety Course or Pharmacovigilance is a better option, as the career in this field can be very satisfying. You might read in newspapers that often many medicines are banned in the market for its contra indications or side effects. How do they arrive at a conclusion that certain drugs have side effects? That is the job of a person who has pursued Drug Safety Course. So, choosing a career in pharmacovigilance can be very satisfying.

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Topics: Drug Safety

Tips for Chemical Inventory Management

Posted by Phil on Jul 26, 2017 1:23:01 PM

Having an organized inventory is the key for your overall chemical management initiatives and adherence to GHS compliance. You should have periodic inventories on what chemicals you have on the site, besides documenting where these chemicals are located, while making sure that accurate and up to date safety data (SDS) is in place.

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Topics: Drug Safety

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