In-vitro Systems Toxicology Approaches for Aerosol based Product Assessment

The principal themes of the academic programme of the Congress are: Toxic deaths; Drugs of misuse; Critical care in poisons cases; Toxicology in specific populations and, finally, a session on the use, usefulness and validity of experimental data in toxicology and the management of patients. There will also be mini-symposia focussing on the Toxicology of anti-diabetic medications, Antidote availability and Veterinary toxicology. Interspersed within these will be a round table session, pro-con debates on hot-topics, and also sessions for discussing recent papers and publications. 

The aim of the course is to give participants an overview of recent advances related to chemical risk management at workplaces. Special emphasis will be in occupational exposure limits and their application at workplaces and the management of special issues like combined exposures, skin exposure, nanoparticles and REACH & OSH interface.

The regulatory acceptance of alternative methods is an ever-evolving area of the 3Rs of toxicology testing and there is a worldwide effort to develop, validate and adopt methods for regulatory submission and product approvals. Three speakers will provide a general overview of alternative methods, including an update on their status of acceptance, with a second focus on recently-validated tests, and finally highlight up-and-coming methods and regulatory challenges.

Pharmaceutics is the discipline that deals with the design and manufacturing of the drug product. Drugs are rarely used only as a pure substance but instead are used in the form of a medicine, i.e. a formulated preparation or a dosage form. This course aims to introduce the various aspects of the administration routes (e.g. oral, nasal, transdermal), the formulation (e.g. liquid, solid, powder) and the manufacturing of medicines. Besides a broad overview about the basic concepts of pharmaceutics in general students will acquire specific knowledge of excipients, dosage forms and their physical constraints as well as understanding of the functions of the several pharmaceutical packagings and devices used for medication. Furthermore the participants will receive knowledge about methods and procedures used in the quality control of medicines, both in development and manufacturing. Lastly, standards of Good Manufacturing Practice (GMP) and regulatory aspects will be part of the course. Further information.

50th anniversary of the SSPT.  

This multidisciplinary congress provides a forum for both internationally established and young researchers to exchange advanced knowledge on Food Contaminants and Human Health. The congress will be comprised of keynote lectures given by world-renowned scholars, in addition to oral and poster sessions. State of the Art developments in different fields of chemical mixtures: analytical chemistry, risk/exposure assesment, bioavailability and toxicity of food contaminants will be covered during presentations.

The SOT Annual Meeting is the largest meeting of its kind. This annual event features a broad range of scientific sessions and a thematic program that provides participants with a unique opportunity to deepen their knowledge in topical areas and interact with leaders in their respective disciplines. The scientific program includes Plenary Lectures and other featured sessions, Symposia, Workshops, Roundtable discussions, Informational Sessions, and a Regional Interest Session, as well as Platform and Poster Sessions. The Society anticipates that more than 6,500 toxicologists from more than 50 countries will attend. The SOT Annual Meeting also includes the ToxExpo, which is the largest exhibition dedicated to toxicology and the biomedical sciences. ToxExpo features 350 exhibitors who lead the industry in developing cutting-edge products, services, and technology to benefit the toxicology community. Exhibitors also have the opportunity to demonstrate their products and educate attendees about their services via Exhibitor-Hosted Sessions throughout the week.

This course is part of DGPT Modular Training Programme in Toxicology and provides a broad overview on the organ systems of interest as well as standard tests to investigate drug effects on these systems. Each organ system will be introduced before detailed information on the safety pharmacology aspects is provided. Integration of Safety Pharmacology findings in an overall risk assessment will be demonstrated. Concordance data and case reports will provide the evidence how meaningful pre-clinical data are for the clinical situation.

This webinar in the Health section of Horizon 2020 shows the numerous funding possibilities for researchers and consortia. 7.2 billion Euros are allocated for health research 2014-2020. A Q&A; session via web chat will be added.  This workshop is free of charge but registration is compulsory.