69.00€
The goal of this course is to bring you specifics of Global Medical Literature Monitoring in pharmacovigilance and one of topic dedicated course among 3 other MLM courses.
This course will give you proper background and knowledge regarding all necessary aspects, practical suggestions and tips which allows you actively involved in this area of Medical Literature Monitoring.
Basically we will discuss regulatory landscape and responsibilities of Marketing Authorization Holder and we will focus on the challenges connected with Global MLM. We will discuss when to start monitoring and when it could be terminated.
We will review specifics of databases and records structure, which should be taken into account during MLM.
We will take a look on database Thesauruses and their added value for the database searching and pharmacovigilance. Balancing of precision and recall will be discussed with focus on creating of query concepts and construction of database query.
I will point out basis of proper process documentation and I will present areas of the process which should be addressed in relevant process documents like SOPs or Working Procedures.
Also Quality assurance in Global MLM will be discussed.
My name is Maciej Szewczyk and I’m CEO of MS Pharm company – pharmacovigilance provider fully dedicated to deliver Medical Literature Monitoring solutions to pharma industry, with strong focus on publications which are not easily reachable – means published locally and in native languages. I’m involved in this area of pharmacovigilance from 2009 on the different positions, from the project management, through business development including designing of dedicated MLM tools to CEO of company which currently manage over 130 MLM projects and cover over 1000 locally published medical and pharmaceutical journals.
I’m very lazy person in that way, that I’m always trying to automatize or at least maximally simplified all repeatable processes. That’s why we develop dedicated MLM tools which allow us to effectively manage projects we are responsible for.
I like to project and involve in development of software, which will make our life easier and more efficient. I love playing with numbers and statistics, that’s why I was involved in preparation of few analysis regarding literature in pharmacovigilance, e.g.
I’m also member of Polish Association of Pharmacovigilance and I was involved in creation of Literature Standard of Polish Association of Pharmacovigilance, which was published in Almanach of Polish Regulatory Authority – Office for Registration of Medicinal Products, Medical Devices and Biocidal Products.
Privately my biggest passion is badminton, skitouring and MTB.
Don’t miss out on this opportunity to revolutionize your employee development process with AIDIFY’s freemium license. Fill out our form to get started today!
Reviews
There are no reviews yet.