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Monthly Archives: October 2019

What are the Career Opportunities for SAS Clinical Course?

The two most important things that people look for in a job include – high pay and better opportunities. This is precisely what the life of SAS Clinical professional is – your route map to higher pay and better growth opportunities.

According to recent findings from research, Clinical SAS is considered to be among the highest valued skills to sustain today’s job market.

But before trying to understand its scope and job opportunities after the Clinical SAS course, it is vital to get to know about the course and the field.

It can be expressed that Clinical SAS is the application of the SAS technology for the analysis of clinical trial data. This procedure is typically employed by clinical and pharmaceutical/biotech companies.

Role of a SAS Programmer in Clinical Field

Industries, including pharmaceutical, clinical research, and biotech companies, use SAS for their clinical trial data analysis. SAS programmers are in-charge of clinical trial data analysis, and they have to manage the received data, control its quality, and ensure its accuracy. The job of SAS programmers also involves the application of analysis methods on gathered data and represents the data listing, graphs, and study summary tables to clinicians and statisticians so they can prepare a study report. The job of SAS programmers is quite similar to that of data managers and statisticians, and they provide a proper link between raw data and analysis.

The job of a SAS Programmer in Clinical Field

SAS analytics have proven to provide accurate data analysis. As a career choice, Clinical         SAS is your definitive path to stay on the top. The combination of familiarity with the aspects of clinical trial and the knowledge of SAS is both rewarding and challenging. Professionals in the field may also gain satisfaction as their contribution positively impacts and transforms a patient’s life. A SAS programmer having Clinical knowledge has a competitive edge as he/she can make their own decisions when programming. Beginning of a Clinical SAS Programming as a clinical programmer will be much profitable as the critical responsibility of a clinical programmer is to write SAS programs to generate proper output required for analyzing and reporting a clinical study. A Clinical SAS Programmer with CDISC expertise is always an added advantage to the organization.

The Clinical SAS training course is your entryway into this rewarding career. Join us for Clinical SAS certification.

A Day in the Life of A Medical Coder ?

People considering Medical Coding and Billing training may keep wondering how their life will turn out to be after getting into the workforce. You may start wondering how your workday would like or worry about the work environment. It is also apparent for you to calculate the pros and cons of Medical Coding and Billing as a career choice?

We understand the enthusiasm and anxiety around it, and we have peeped into the life of a medical coder to understand their typical day at work; and here is what we have learned –

The start of their day

A typical workday of a medical coder starts with them sitting in front of their desks. They have to log-in to the software system to check out the tasks they have to work on. They usually get charts showing diagnoses and medical procedures performed, and the professional has to review them. It is the job of a coder to assign medical codes to the diagnoses and procedures. There are two major coding systems – Current Procedural Terminology (CPT) and International Classification of Diseases (ICD-10). Professionals learn these systems during their medical coding and billing training program. For a medical coder, there is nothing more important than being accurate about coding.

Coders will have to renew both straightforward as well as robust charts. Medical coders also come across medical charts with missing documentation. In such cases, the medical coder needs to email the doctor before the coding can be done to make accurate entries. In these cases, coders usually feel like detectives at work trying to solve a case.

The work station

The work station of a medical coder depends on the employer. It usually involves individual cubicles or shared desks with two monitors – one for accessing the patient chart, and the other for researching and coding systems. Medical coders will have to work in a demanding where they are expected to finish reviewing a certain number of charts/day.


The number of medical coders in a team/ organisation will again depend on the employer and the type of job. For a professional coder working in a major hospital, there will be dozens of medical coders in the team. Working with a group serves as a great advantage when dealing with problems in a chart. On the other hand, smaller private medical offices hire medical coders. In such cases, the coder count is meager.

So this is how you can expect your life as a Medical Coder. We wish you the best of luck in this career field!

Pharmacovigilance: 4 Key Challenges

The field of Pharmacovigilance focuses on quality of a drug, adverse effects associated with it, and medication errors, impacting the health care system. According to the definition put forward by WHO, pharmacovigilance can be defined as “the science and activities relating to the detection, assessment, understanding, and prevention of adverse effects or any other medicine-related problem”.

For the uninitiated, pharmacovigilance is the constant process which involves identification and monitoring of the safe use of pharmaceutical products. The process thus helps minimize the risk of possible harm coming to the patients. As a part of their duty, Pharma Companies are compelled to conduct a pharmacovigilance and comprehensive drug safety audit to see if the proposed product is compliant with FDA guidance, and worldwide laws and regulations.

This article discusses few challenges to Pharmacovigilance –

1. Inconsistent reporting of the adverse effects

The biggest challenge of pharmacovigilance is the inconsistent reporting of the adverse effects. It is important to understand that adverse effects associated to a drug or a medical device may occur not only during a visit to the Healthcare Center, but even after a few hours after the drug adminstration. Patients often fail to remember or notice adverse events experienced and this leads to inconsistent reporting. There are other cases where the patients feel anxious and report discomfort as adverse events. Such wrong reporting leads to incorrect conclusions which further result in the withdrawal or suspension of drugs.

2. Challenges of spontaneous reporting

Patients or drug companies may voluntarily come forward to report adverse events, but under-reporting impact the post-marketing databases. It may also be observed that medical staff neglect reporting and avoid reporting the symptoms which they feel are not serious. This can sometimes lead to delay in the focus towards potential serious adverse events (which might differ from patient to patient) that require immediate action. When the effects of a drug or medical device are not reported spontaneously, then there may be a problem while marketing and distribution.

Another major problem in pharmacovigilance is due to miscoding and misreporting of the adverse events. The field of pharmacovigilance is all about formulations, dosage, time and length of the exposure to adverse effects, and when these elements aren’t reported properly, it becomes difficult to manage and analyze the data. This may also result in false alarms for adverse effents that are non-existent.

3. Priority of efficacy over safety

Smaller or new age drug companies tend to focus more on efficacy over safety during clinical trials and this results in the compromise in drug quality. It is important for such companies to understand that drug development depends on the balance between efficacy and safety.

4. Limitations in Published case reports

The best way to alert about the adverse effects of drugs or medical devices is by publishing detailed reports in medical journals. This is an efficient way to convey suspected adverse effects and drug hazards. However, only a small number of such cases are published, and the reports published regarding them are poorly documented. There are a few cases where there are delays in reports indicating the publication and occurrence of adverse events.

Pharmacovigilance as a career path offers bright future. The field has a lot of demand and it is evolving by the day. Hyderabad, the city known for being professional hub, hosts several pharmacovigilance training centers in its heart land – Ameerpet. For people looking for the best pharmacovigilance training center in Hyderabad, Joshi Medicode is the right place to get trained.

Along with the best pharmacovigilance training, Joshi Medicode also offers medical coding and billing courses including ICD-10 and Clinical SAS courses.

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