67377 Courses

RYA Diesel Engine

4.9(48)

By Go West Sailing

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.

RYA Diesel Engine
Delivered In-PersonFlexible Dates
£99

RYA Radar

4.9(48)

By Go West Sailing

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

RYA Radar
Delivered In-PersonFlexible Dates
£99

CT01: How to Gain and Maintain Approval for Clinical Research Under the EU Clinical Trials Directive

By Zenosis

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.

CT01: How to Gain and Maintain Approval for Clinical Research Under the EU Clinical Trials Directive
Delivered Online On Demand3 hours
£149

CT03: ICH Good Clinical Practice

By Zenosis

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.

CT03: ICH Good Clinical Practice
Delivered Online On Demand3 hours
£149

First Aid for Dentists including 6 hours Verifiable Enhanced CPD

5.0(1)

By First Aid for Life

First Aid for Dentists including 6 hours Verifiable Enhanced CPD
Delivered Online On Demand6 hours
£149

PV03: Drug Safety and Pharmacovigilance

By Zenosis

Drug safety monitoring and risk management are vitally important for medicinal product developers, licence holders and clinical investigators. In addition to their duty to protect public health, increasingly tight regulation and potentially massive payments to litigants provide strong incentives for pharmaceutical and biotechnology companies to ensure that they maintain efficient systems for drug safety / pharmacovigilance and that all staff are aware of the basic requirements. This course will provide them with an overview of the most important aspects of this discipline, both before and after marketing of products, especially as they apply in Europe and the USA.

PV03: Drug Safety and Pharmacovigilance
Delivered Online On Demand2 hours
£149

Studyhub Lifetime Prime Membership

5.0(2)

By Studyhub UK

Studyhub Lifetime Prime Membership
Delivered Online On Demand
£149

CT10: The Investigational New Drug Application (IND) to Conduct FDA-regulated Clinical Trials

By Zenosis

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.

CT10: The Investigational New Drug Application (IND) to Conduct FDA-regulated Clinical Trials
Delivered Online On Demand3 hours
£149

Electrician: Electrical Training & Electrical Engineering Career Based Job Focused Program

5.0(10)

By Apex Learning

Advance your career with the Electrician: Electrical Training & Electrical Engineering Career-Based Program. Enroll today to unlock job-focused training and enhance your employability!

Electrician: Electrical Training & Electrical Engineering Career Based Job Focused Program
Delivered Online On Demand25 hours
£149

Supply Chain Management, Purchasing, Logistics management & Retail Management - 30 Courses Bundle

By NextGen Learning

Supply Chain Management, Purchasing, Logistics management & Retail Management - 30 Courses Bundle
Delivered Online On Demand5 days
£199