67030 Courses

RYA first aid, sail training, first aid at sea course, 1st aid training

A one-day/8 hour course, you will leave being aware of the main systems of a marine diesel engine. With a focus on prevention of breakdown at sea and having an ability to resolve defects which do not require workshop support. Course topics include: The four stroke cycle, Fuel, cooling and air systems, Engine electrical systems, Spares and tool requirements, Winterisation and servicing Course materials and tea and coffee are included in the price.

A one-day/8 hour radar navigation course giving you an understanding of radar as an aid to navigation and collision avoidance. Cruising boats increasingly have radar on board. The International Regulations for the Prevention of Collisions at Sea state that if you have a radar, you must know how to use it. Radar is probably the most versatile of all electronic navigation aids, but the best results are only obtained when you know how to use all the functions correctly. It is not an automatic all-seeing eye, and can easily mislead those who do not understand its controls, allow for its limitations, or interpret its picture. Course topics include: how the radar set works how its adjustments and features affect the way it works target definition radar reflectors types of radar display radar plotting the use of radar in navigation and collision avoidance Course materials included in the price: RYA student pack - Radar Course Questions and Answers RYA booklet - An introduction to Radar

To conduct a clinical trial in the European Economic Area under the Clinical Trials Directive the sponsor must apply for authorisation from the national competent authority (i.e. medicines regulator), and favourable opinion must be obtained from a research ethics committee, in each member state in which the trial is to take place. This module sets out the requirements for successful compilation, submission and maintenance of the applications.

An Investigational New Drug Application (IND) is a submission to the US Food and Drug Administration (FDA) for permission to conduct a clinical trial of a medicinal product. This module describes regulatory requirements that sponsors or sponsor-investigators must meet for successful compilation, filing and maintenance of INDs. The IND and its role are defined, and the contexts in which it is required are specified.

Good Clinical Practice (GCP) is a set of internationally recognised ethical and scientific quality requirements for designing, conducting, recording and reporting clinical trials. Compliance with GCP principles is required by regulatory authorities in many countries for the authorisation of clinical trials and the acceptance of their data. The International Council for Harmonisation’s guideline E6, often referred to as ICH GCP, is the international standard specification for Good Clinical Practice.