Teaching Program 2021-2023

FIRST YEAR – First semester (all students) 

  1. Anatomy and physiology of skin and appendages. The students will learn anatomy and histology of skin and appendages and the physiological mechanisms regulating the integumentary system (see details).


  1. Pathological mechanisms of skin disorders. The students will learn the basis of mucosal immunity, the pathogenesis of inflammatory skin disorders, either autoimmune disorders or allergies, and the cellular and molecular mechanisms underlying wound healing. The students will also gain knowledge on the physiological microbiota of skin and on the principal pathogens associated with skin diseases (see details).


  1. Statistics, data retrieval, data mining and epidemiology. The students will gather basic information on statistics for the biomedical sciences, will be taught how to retrieve, categorize and use information both in a supervised and unsupervised manner. This will include the know-how to perform systematic reviews of the literature and meta-analysis as well as the basic principles of epidemiology to understand the therapeutic need. These topics will be consolidated through examples and computer exercises (see details).


  1. The pillars of drug discovery and development (I). The course delivers information on the drug discovery and development process providing the general principles of R&D. It will be divided in sub-courses:

(i) Introduction to the general principles of R&D and translational skills (including project management, decision making, communication skills, intellectual property, trademark protection and good practices) (see details).

(ii) Organic Chemistry. The students will be introduced to the main functional groups and heterocycles, their electronic properties and reactivity. Selected examples of synthetic routes to pharmaceutical and cosmetic compounds will be illustrated (see details).

(iii) Natural products. What is a natural product and how to distinguish natural products from their synthetic version? Plant natural product biosynthesis. Plant biotechnology to produce natural products. Terpenes, alkaloids, flavonoids. Aromas and fragrances (see details).

(iv) Protein Science and biotechnology. The course will provide the rudimental of biotechnology and protein science and elaborate around the central concept of protein structure-function relationship. Selected biotechnological techniques used in protein science will be reviewed and examples of proteins of pharmaceutical interest for translational cosmetic and dermatological science will be presented (see details).


The mark will be obtained by the weighted average of the grades obtained in the four parts that compose the exam. All the four parts have to be passed with a grade of at least 18. In case that this does not occur, the student will have to resit the exam. He/she will have to retake only those partial exams that were not passed or those for which the mark was refused in the first session while the other marks will be retained.


  1. General principles of drug and cosmetic regulation. This unit focuses on the main issues regarding regulations and the distinction between the pharmaceutical and the cosmetic world and the different geographical regions (see details).


FIRST YEAR – Second semester (all students)

  1. The pillars of drug discovery and development (II). The course delivers information on the drug discovery and development process providing the general principles of R&D. It will be divided in sub-courses:

(i) Pre-clinical and Clinical Pharmacology. The course will illustrate the drug discovery process from a pharmacological perspective and will provide students with notions of the main drug classes. The course will also provide students with the ability to read and critically analyse pre-clinical and clinical data(see details).

(ii) Medicinal Chemistry. The course will provide the students with the basic principles for the discovery and optimization of a bioactive compound, from hit to lead, with a focus on drug metabolism. The design of prodrugs and softdrugs for topical use will be covered. Examples of successful stories of dermatological drugs will be presented (see details).

(iii) In silico drug discovery and design. The course will illustrate the many ways we can describe, represent and visualize molecules in the computer, the importance of recognizing and understanding the concept of similarity and the physicochemical and topological descriptors. The students will learn the use of chemoinformatics approaches and virtual screening as an example to identify molecular structures with potential biological activity (see details).

(iv) Principles of formulation. The course will provide students with basic principles of formulation, illustrating how physical pharmacy principles are applied to the preparation of liquid and semi-solid dosage forms used for topical application of medications and cosmetics (creams, ointments, gels, colloids, patches and sunscreen formulations) (see details).

The mark will be obtained by the weighted average of the grades obtained in the four parts that compose the exam. All the four parts have to be passed with a grade of at least 18. In case that this does not occur, the student will have to resit the exam. He/she will have to retake only those partial exams that were not passed or those for which the mark was refused in the first session while the other marks will be retained.


  1. Principles of dermatological symptoms and of skin aging. The students receive knowledge on the dermatological symptoms, and the clinical features of disorders, including skin photo-ageing and photoprotection. The course will highlight the current unmet medical needs (see details).


  1. Strategies for the synthesis, extraction of novel compounds, formulation and analysis of dermatological products. This course makes use of formal lectures as well as of experiments in laboratory. At the end of this course, students will be able to conduct a synthesis, from the setup of the reaction to the purification of the product, to perform extraction and distillation of natural sources, formulate a dermatological product, evaluate its quality and interpret data. In particular, students will be provided with:

(i) the main safety principles and techniques used for the synthesis of organic compounds (reaction setup, product isolation and purification);

(ii) the principles and techniques for the isolation of organic compounds from their natural sources;

(iii) the techniques for the formulation of cosmetic and dermatological products;

(iv) The key areas of quality control of cosmetic and dermatological products: quality assessment during products development (Quality by Design); implementation of stability testing of active pharmaceutical ingredients (APIs) and finished products; determination of APIs retesting period, drug products shelf-life, and storage conditions; regulatory guidance;  key principles of high performance liquid chromatographic (HPLC) analysis, development of analytical methods and validation (see details).


SECOND YEAR – First semester

 Option A – Cosmetic and Pharmaceutical Research (half of the students)

  1. Cosmetic and dermatological products on the market; from molecular biology to market. At the end of the course the student will be provided with the principles for developing bioactive molecules into products based on solid science that includes the use of biotechnology-derived ingredients, genetic profiling for individual skin-care, stem-cell-based products and therapies to regenerate ageing tissues, or cell and tissue engineering. In addition, the course will also concentrate on market penetration, value proposition and  value development of products (see details).
  1. In vitro skin models for testing and evaluation. The main aim of this course is to provide the knowledge necessary to design, develop and validate bioactive compounds from library screenings to cosmetic and dermatological applications to obtain effective and stable products for exploitation. At the end of the laboratory, the students will be familiar with the most up-to-date cellular and multicellular in vitro models employed to assess the efficacy, safety, and mechanism of action of bioactive molecules and other ingredients (see details).
  1. Safety Evaluation. The course will address potential off-target effects as well as knowledge on how to perform safety assessments and toxicological profiles of cosmetic and dermatological products, evaluating the risks of their application to healthy human skin under normal and foreseeable use conditions (see details).
  1. Pre-clinical regulatory and quality compliance issues world-wide. The student will be provided with the main laws and regulations for cosmetics and drugs for exploitation, including good laboratory and manufacturing practices, requirements for registration, and labelling (see details). 
  1. Scientific skills in preclinical studies. The student at the end of the course will be able to cope with the scientific literature and with writing a scientific paper, divulgate and marketing skills (see details).


Option B – Clinical Development

(UNamur, half of the students)

1. Clinical trials. The student will get an overview of the entire process of Clinical Drug Development. The current rules and regulations are explained and put into a historical perspective. The course will teach how the different actors are involved in clinical drug research, about the respective roles and the way they interact between one another. Through some practical exercises and visits to phase 1, CRO and pharmaceutical companies, the student will have a better insight on how medications are distributed, stored and administered to subjects, how the coordination in Clinical Trials Centres occurs and what the different source documents look like. The course will discuss some ethical questions, new trends in Clinical Development, innovative ways to recruit subjects in Clinical trials, adaptive designs, concept of Lean and the latest trends in Clinical research. It will also tackle the new European Regulation on Clinical trials (see details).

2. Quality assurance: GMP, GCP, GLP and auditing. The principles of quality assurance in the field of healthcare and drug development are depicted. The international standard ISO17025 is reviewed in detail to give a complete overview of a quality system with organizational and technical requirements. The different GxP standards will be covered: GLP (good laboratory practices) for the pre-clinical studies; GCP (good clinical practices) and GCLP (good clinical laboratory practices) for the clinical studies; GMP (good manufacturing practices) and GDP (good distribution practices) for drug production and distribution. Finally, the students will be introduced to the concept of validation in the broad sense of the term, to cover all the topics concerned by qualification or validation needs (equipment, process, methods, IT systems….). (see details)

3. Bioethics. This course will illustrate the ethical requirements for the conduction of clinical trials in contemporary science, also giving an overview of historical pillars that brought legislations and opinions to change (see details).

4. Clinical study management. This course puts emphasis in the practice of the theoretical concepts. The role of clinical study manager will be explained. Applicable software system used by biotechnology and pharmaceutical industries will be explained as well, with focus on planning, performing and reporting functions, along with participant contact information, tracking deadlines and milestones. The course we highlight the following topics: efficient recruitment of trial participants; the importance of education and experienced study personnel; publication of trial results and dissemination (see details).

5. Clinical research associate training. The course will provide students with the basic training required for clinical research associates. The course has the added value of allowing students to undertake an internship in a clinical research organization according to EU legislation, if in their will (see details).

6. Clinical project management. The students will be introduced to the role, skills and responsibilities of a Clinical Project Manager (hard skills, soft skills and how to optimize clinical trials). (see details)

7. Biomarkers and surrogate markers in clinical dermatology trials.
The course will teach how to discriminate a biomarker from a surrogate marker in the context of regulatory affairs and their importance in the interpretation of clinical trials in dermatology. (see details).

8. Lecture series in dermato-cosmetic sciences.
Lectures in the field of dermato-cosmetology will be given with a focus on basic and translational research & development, and regulatory affairs. Each year, a couple of companies are invited to introduce their recent R&D developments. (see details).



Size, characteristics and peculiarities of the dermatological and cosmetic markets (Italy, 2 ECTS). This workshop will introduce students to the pharmaceutical and cosmetic industry, the main areas of investment of companies as well as to the world of marketing. Dedicated lectures on marketing strategies, social communication, digital commerce and social data enrichment will be delivered, alongside lectures that illustrate size and characteristics of the different markets. The workshop will be held in September, during the induction week.

Download here the program for the workshop.

Download here the program for the induction week.

The evaluation of the workshop will be based on the participation in a science dissemination project that includes the website run by EMOTION students (http://emotion-master-studentproject.eu/).

Communication and Job Seeking Skills (Belgium, 3 ECTS). At the end of the workshop participants will be able to set up and manage a personal strategy for job searching. The intensive programme provides participants with the insights and skills to: (i) understand and explore recruitment tools and channels; (ii) improve their understanding of personal proposition; (iii) develop a more strategic approach to job searching and networking; (iv) plan a process to manage career step; (v) better understand and use the principles of human resources relations; (vi) practical exercises. Part of the time will also be reserved to the presentations by students on their Case Study.

Business Plan and Entrepreneurship (Spain, 3 ECTS). The students will receive lectures from non-academic professionals relating to the ideation and construction of businesses centred on cosmetic and pharmaceutical products, with examples of success stories as well as failures. Part of the time will also be reserved to the presentations by students on their Business Plan and on their Clinical Trial.



Case Study and Project Management (First year, second semester,  4 ECTS). The course will run with tutors. Students will be given a cosmetic or pharmaceutical product and they will need to explore: (i) the biological potential; (ii) the marketing potential; (iii) the literature that supports any claims; (iv) to propose a strategy for marketing the product; and (v) to provide R&D programmes for follow-on products and for life-cycle management. The course will also use flipped classroom techniques by which students will be required to work in teams. The Case Study will be presented by the students during one of the workshops.

Starting up a company: the Business Plan (Second year, first semester, Option A,  4 ECTS). Students, working in groups, will be required to develop a business plan for a potential new company they would like to set-up around their interests. They will receive tutoring on the scientific and business aspects of the project. The project will culminate at the end of the semester during one of the workshops in a pitch delivered to non-academic professionals that will play the role of investors.

What is intellectual property and how to protect it (Second year, first semester, Option A, 3 ECTS). The students will learn the conditions for discovery, intellectual property rights and patenting. The structure of a patent application will be reviewed and concepts such as objective novelty, priority principle and inventive step will be reviewed and illustrated with examples. Emphasis will be on principles and strategies in connection with preparing patent applications, with weight on types of requirements and their formulation. Various illustrative case stories will be reviewed and worked on in groups, and students will then present their results.

A case study of clinical trial (Second year, first semester, Option B, 4 ECTS). Students will be asked to design a clinical development (Phase I, Phase II, and Phase III study) for a drug which has just completed pre-clinical investigations. Students will be divided in small groups (2-3). The Case Study will be presented during one of the workshops.



During the fourth semester, Students will complete an elective project in industry or at a research laboratory (30 ECTS). The traineeship lasts 22 to 26 weeks.

Last modified: January 9, 2023