I have thoroughly read the admission requirements and believe that I meet both the basic
requirements as well as the academic basis for admission to the specific master's program. In this self-assessment paper, I will elaborate on my knowledge and competency during my previous studies and employment.
Firstly, as I aforementioned I received my bachelor's degree in Pharmacy and master's degree in Pharmaceutical chemistry gaining an honor diploma and being top of the faculty. During these years of study, I deeply learned the subjects that are directly applicable to the curriculum of the Master’s Programme in Pharmaceutical Research, Development, and Safety. Some of these subjects are as follows:
Organic chemistry
Pharmaceutical chemistry
Pharmacology and Clinical Pharmacology
Pharmaceutical biotechnology
Pharmaceutical engineering
Drug metabolism
Chemical drugs
Additionally, my bachelor's and master's thesis subjects were research-oriented and required excellent lab skills. "The application of Spectrophotometry in Pharmaceutical Analysis" and “The analysis of several drugs containing phenolic compounds with High-performance liquid chromatography”, respectively. I am confident that these skills will assist me during my future thesis preparation and defense.
When it comes to professional skills that I earned during my approximately five years of work experience, the regulatory affairs specialist position in the Analytical Expertise Center PLE, MOH, national regulatory agency, is the particularly relevant background for the Medication safety and effectiveness study track. During my employment, I learned national and international guidelines on state registration of drug products and evaluated dossiers submitted to state registration and reregistration that can apply to the course of the Marketing authorization of drug products and pharmacovigilance.
When it comes to professional skills that I earned during my approximately five years of work experience, the regulatory affairs specialist position in the Analytical Expertise Center PLE, MOH, national regulatory agency, is the particularly relevant background for the Medication safety and effectiveness study track. During my employment, I learned national and international guidelines on state registration of drug products and evaluated dossiers submitted to state registration and reregistration that can apply to the course of the Marketing authorization of drug products and pharmacovigilance.
I have
thoroughly
read the admission requirements and believe that I
meet
both the basic
requirements
as well as
the academic basis for admission to the specific master's program. In this self-assessment paper, I will elaborate on my knowledge and competency during my previous
studies
and employment.
Firstly
, as I aforementioned I received my bachelor's degree in Pharmacy and master's degree in Pharmaceutical chemistry gaining an honor diploma and being top of the faculty. During these years of
study
, I
deeply
learned the subjects that are
directly
applicable to the curriculum of the Master’s
Programme
in Pharmaceutical Research, Development, and Safety.
Some
of these subjects are as follows:
Organic chemistry
Pharmaceutical chemistry
Pharmacology and Clinical Pharmacology
Pharmaceutical biotechnology
Pharmaceutical engineering
Drug metabolism
Chemical drugs
Additionally
, my bachelor's and master's thesis subjects were research-oriented and required excellent lab
skills
.
"
The application of
Spectrophotometry
in Pharmaceutical Analysis
"
and “The analysis of several
drugs
containing phenolic compounds with High-performance liquid chromatography”,
respectively
. I am confident that these
skills
will assist me during my future thesis preparation and defense.
When it
comes
to professional
skills
that I earned during my approximately five years of work experience, the
regulatory
affairs specialist position in the Analytical Expertise Center PLE, MOH,
national
regulatory
agency, is the
particularly
relevant background for the Medication safety and effectiveness
study
track
. During my employment, I learned
national
and international guidelines on
state
registration
of
drug
products
and evaluated dossiers submitted to
state
registration
and
reregistration
that can apply to the course of the Marketing authorization of
drug
products
and
pharmacovigilance
.
When it
comes
to professional
skills
that I earned during my approximately five years of work experience, the
regulatory
affairs specialist position in the Analytical Expertise Center PLE, MOH,
national
regulatory
agency, is the
particularly
relevant background for the Medication safety and effectiveness
study
track
. During my employment, I learned
national
and international guidelines on
state
registration
of
drug
products
and evaluated dossiers submitted to
state
registration
and
reregistration
that can apply to the course of the Marketing authorization of
drug
products
and
pharmacovigilance
.