8792 Courses delivered Online

Level 5 Diploma in Education and Training (RQF)

By Sirius Group Training

Are you passionate about education and eager to take your teaching career to the next level? Look no further! Our Level 5 Diploma in Education and Training (RQF) is designed to empower educators like you with the knowledge and skills needed to excel in the ever-evolving field of education.

Level 5 Diploma in Education and Training (RQF)
Delivered Online On Demand1 hour
£1500

Writing and Managing Requirements Documents - Creating the Acceptable, Approvable Requirements Document: On-Demand

By IIL Europe Ltd

Writing and Managing Requirements Documents - Creating the Acceptable, Approvable Requirements Document: On-Demand
Delivered Online On Demand7 hours
£850

Developing the Business Case - Defining the Business Problem and Solution Scope: On-Demand

By IIL Europe Ltd

Developing the Business Case - Defining the Business Problem and Solution Scope: On-Demand
Delivered Online On Demand12 hours
£850

Politics and Project Management - Turn Project Politics into a Positive Force for Project Objectives: On-Demand

By IIL Europe Ltd

Politics and Project Management - Turn Project Politics into a Positive Force for Project Objectives: On-Demand
Delivered Online On Demand15 minutes
£850

SUB12: Registration of Medicinal Products Based on Monoclonal Antibodies

By Zenosis

This module addresses characteristic issues influencing the registration of medicinal products based on monoclonal antibodies (mAbs), for use in humans. Regulatory requirements for the registration of biological medicinal products such as those based on mAbs differ in certain respects from those for small-molecule products. This is because of the distinct characteristics of biologics, such as complex structure and susceptibility to variation during manufacture.

SUB12: Registration of Medicinal Products Based on Monoclonal Antibodies
Delivered Online On Demand1 hour 30 minutes
£74

SUB04: Preparing Submissions in the Common Technical Document (CTD) Format

By Zenosis

The CTD is the internationally recognised standard format for submissions to medicines regulatory authorities. In the European Economic Area, the USA and Canada, the CTD, in its electronic format (eCTD), is mandatory for all applications for marketing approval and all subsequent related submissions. The CTD is accepted in many other countries, being mandatory for new prescription medicines in some. This module explains the rationale for the CTD and provides guidance on its structure and format and the ways in which it is used.

SUB04: Preparing Submissions in the Common Technical Document (CTD) Format
Delivered Online On Demand1 hour 30 minutes
£74

Level 3 Learning & Development Practitioner

By Cavity Dental Training

Level 3 Learning & Development Practitioner
Delivered OnlineFlexible Dates
£209 to £2500

SQL Querying Fundamentals - Part 1

By Nexus Human

SQL Querying Fundamentals - Part 1
Delivered OnlineFlexible Dates
£495

Scrum Master Exam Prep: Virtual In-House Training

By IIL Europe Ltd

Scrum Master Exam Prep: Virtual In-House Training
Delivered OnlineFlexible Dates
£850

Managing Multiple Projects: Virtual In-House Training

By IIL Europe Ltd

Managing Multiple Projects: Virtual In-House Training
Delivered OnlineFlexible Dates
£850