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Our certificate courses take place within the master year 1 or year 2 curriculum schedule.
Therefore, some may be available for application, while others might be temporarily closed. In the latter case, please see the course details for the next application periods.
OPEN FOR APPLICATION
METHODS IN CLINICAL RESEARCH, PHARMACOEPIDEMIOLOGY AND IN THE ASSESSMENT OF THE EFFICACY OF MEDICINES
Learn how to design clinical trials and analyse clinical research
PHARMACOVIGILANCE REGULATORY PROCESSES
Understand the regulatory requirements and best practices for the Pharmaceutical Industry operational aspects of pharmacovigilance
FUNDAMENTALS OF QUANTITATIVE BENEFIT-RISK ASSESSMENT METHODS IN DECISION MAKING ON MEDICINES
Learn how to evaluate quantitative benefit-risk assessment to help in the decision-making process on medicines
PRINCIPLES OF PHARMACOECONOMICS AND VALUATION OF HEALTH STATES
Learn to evaluate (and design, for the extended version of this module) all relevant aspects of pharmacoeconomic evaluation studies.
DRUG UTILISATION STUDIES: QUALITATIVE METHODS
Learn how to evaluate and design qualitative drug utilisation studies
KEY ROLES AND STAKEHOLDERS IN MEDICINES RISK COMMUNICATION: DUTIES AND CHALLENGES
Learn about strategies to address the main challenges of medicines risk communication
BASICS IN EPIDEMIOLOGY
Get familiar with epidemiology and its application to medicines surveillance
BASICS IN STATISTICS
Get familiar with statistics and their use in epidemiological studies
BASICS IN MEDICINES RISK COMMUNICATION
Get introducted to the basics of communication and medicines risk communication
SUBSTANTIATION AND QUANTIFICATION OF RISKS
Understand and assist in pharmacoepidemiological studies using large healthcare databases
CRITICAL APPRAISAL OF CLINICAL TRIALS: EVIDENCE-BASED MEDICINE AND ITS UNCERTAINTIES
Be conscious of how to apply the results of clinical trials on making therapeutic decisions
IDENTIFYING ADR SUSCEPTIBILITY AND VARIATION IN DRUG RESPONSE
Learn pharmacogenetic successes and failures and be aware of potential limitations of pharmacogenetic results
ADVANCED QUANTITATIVE BENEFIT-RISK ASSESSMENT METHODS IN DECISION MAKING ON MEDICINES
Get expert in quantitative benefit-assessment impact on different decision makers at different phases of drug development
THE PUBLIC HEALTH IMPACT OF ADVERSE DRUG REACTIONS
Learn how to evaluate the public health impact of selected adverse drug reactions from experimental and observational studies
CURRENTLY CLOSED FOR APPLICATION
Check the course details for the next application periods.
CLINICAL AND PHARMACOLOGICAL PRINCIPLES
Be aware of the different sources of information used by physicians to prescribe medicines
PHARMACOVIGILANCE REGULATIONS
Get familiar with the EU, US and major local and worldwide pharmacovigilance regulations and guidelines
PRINCIPLES OF IDENTIFYING AND RECOGNIZING ADVERSE EVENTS AND SAFETY SIGNALS
Get familiar with adverse drug reactions, safety signals and how to handle them
DRUG UTILISATION STUDIES: INTRODUCTION AND QUANTITATIVE METHODS
Learn how to evaluate and design quantitative drug utilisation studies
INFORMATION AND COMMUNICATION ABOUT BENEFIT-RISK OF MEDICINES. BASIC PRINCIPLES.
Get deeper in the medicines risk communication: stakeholders, media, regulations
INTRODUCTION TO BENEFIT-RISK ASSESSMENT AND PHARMACOECONOMICS IN DECISION MAKING
Understand the role of benefit-risk assessment and pharmacoeconomics in the process of decision-making on medicines by different stakeholders
BASICS IN CLINICAL PHARMACOLOGY
Recognise the main issues of Randomised Clinical Trials (RCT), their strengths and weaknesses
PRINCIPLES OF PHARMACOVIGILANCE
Understand pharmacovigilance principles and stakeholders during medicines lifecycle
BASICS IN PHARMACOEPIDEMIOLOGY
Know the real use of a medicine as compared to the "theoretical" indication it was intended and studied for
BASIC PHARMACOVIGILANCE AND PHARMACOVIGILANCE REGULATIONS
Let us guide you through the Basic Pharmacovigilance and Pharmacovigilance Regulations topics and get the necessary knowledge and skills to do it right
PHARMACOVIGILANCE FOR BIOLOGICS
Let us guide you through the Pharmacovigilance for Biologics topic and get the necessary knowledge and skills to do it right
EXTERNAL DATABASES - RWD - RWE
Let us guide you through the External databases/RWD/RWE topic and get the necessary knowledge and skills to do it right
