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Chat NowIf you find the clinical research field challenging, well, in that case, this is the best course for you. We provide 3 Modules Pharmacovigilance, Clinical Data Management and Clinical Research in this course.
PHARMACOVIGILANCE:
-here in this course I will provided excellent material for pharmacovigilance and there is very important interview questions and answers also. Don't miss the valuable material. pharmacovigilance course. Even rural background students also understand the language mentioned in this material. All the best.
- pharmacovigilance is a continuous process accepted for safety evaluation accompanied by steps to improve safe usage of medicines. pharmacovigilance course
-pharmacovigilance is considered to be one of the best career option for life science and pharmacy graduates. pharmacovigilance course. It mainly deals with reporting and analysing of medicine side effects and ensure drugs in the market are safe and secured
-pharmacovigilance associate salary in india for freshers ranges between 2.2 lakhs to 5.0 lakhs with an average annual salary of 3.3 lakhs.
-the principal goal of pharmacovigilance is to influence safer usage of medicines. pharmacovigilance course. But, it faces increasing pressure to analyze more data sooner, monitor risks more broadly, and accurately report patient events globally.
-pharmacovigilance is regarded as a great career option for interested aspirants as it reflects a well-defined and growing career path. pharmacovigilance course, There is a faster career growth leading to managerial as well as director roles eventually along with a quite decent salary package. pharmacovigilance course. Here, in this article, we have highlighted different curriculum and career aspects of pharmacovigilance. For someone willing to initiate his/her career in pharmacovigilance, the entry-level job is that of a drug safety associate (dsa). All dsas get involved in developing various cases, checking for minimum safety information (msi), reconciliation and then following up processes, along with data entry of all information available in the document and medical coding.
Eligibility criteria for pharmacovigilance
for aspirants to undertake a professional career in pharmacovigilance, the minimum eligibility conditions for applying for the course are as follows:
graduate or postgraduate degree in chemistry (subject) with securing at least 50% marks in aggregate
graduate or postgraduate degree in pharmacy or pharmaceutical sciences
graduate or postgraduate degree in medicine
the process of selection for the course is completely based on merit. Students are granted admission only if they have cleared a written examination followed by a personal interview.
CDM:
this course is designed to introduce the concept of clinical data management and data management activities for beginners in healthcare industry
Section 1 starts with an overview of clinical data management, discussing what is clinical data management and regulations, standards implemented in cdm. clinical data management course
Section 2 outlines cdm process, data management plan and describe activities involved in different phases of data management. clinical data management course
Section 3 gives an overview of variable tools used in cdm and key members involved in cdm team with their responsibilities, clinical data management course
at the end of the course, you will able to
understand clinical data management and it's role in clinical research
clinical data management course describe activities involved in cdm process
demonstrate functions of key members in cdm and variable tools available for cdm, clinical data management course
CLINICAL RESEARCH:
The pharmaceutical industry is one of the extremely regulated industries, with several government regulations to protect public health. clinical research, Therefore, the important target of the pharmaceutical industry is to develop a drug product passing the regulatory requirements. On the other hand, regulation of drug development, manufacturing, marketing, and sales involves paradoxical objectives. clinical research. It must ensure that safe and effective pharmaceutical formulations reach the public quickly while concurrently protecting against ineffective/unsafe/harmful therapies. clinical research course will provide you with a strong understanding of the drug development process, clinical research and related documents, gcp, roles, and responsibilities of major players in clinical research in a summarized manner which will help to work towards shaping your career in clinical research.
This course focuses on the following points that could make clinical research activities smooth without any significant delays/failures,
basic understanding of clinical research,
major players in clinical research,
historical background of us drug law and regulations,
drug approval process,
new drug development-preclinical steps
investigational new drug application (inda),
new drug application (nda),
abbreviated new drug application (anda),
essential documents,
protocol,
source documents,
informed consent form,
investigators brochure,
case report form (crf),
inclusion-exclusion criteria,
sponsor,
investigator,
clinical research associate (cra) and clinical research coordinator (crc),
important literature search websites for clinical research professional,
many more...
There will be several downloadable documents so that you can follow along with them whenever you need them.
This course contains commonly asked questions that will help you while preparing for clinical research interviews.
Last but not the least, this course also contains a bonus course entitled "meeting etiquettes" which will help you to shape your career in which the points that must be taken into consideration while attending/conducting meetings are covered.
In this course, more than 30 informative videos are included and are designed in an easily digestible format and going to take you through step by step approach to understand clinical research and relevant activities.
I believe "quality improvement is a continuous and lifetime process". clinical research, Upon completion of this course, you will be a whole different professional with improved clinical research knowledge which will help you to garner more respect from your team members, managers, clients, or anyone with whom you are communicating/interacting.
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