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1320 Courses

55238 SharePoint Online for Administrators

By Nexus Human

55238 SharePoint Online for Administrators
Delivered OnlineMon, Nov 2513:00 + more
£1785

NCSP Digital Business Risk Awareness Training

By IIL Europe Ltd

NCSP Digital Business Risk Awareness Training
Delivered OnlineFlexible Dates
£200 to £695

ESS01: Essentials of EU and US Regulatory Affairs for Human Medicinal Products

By Zenosis

This foundation-level module is the ideal introduction for new entrants to the field of pharmaceutical regulatory affairs and compliance. It describes the principal requirements that must be satisfied to gain and maintain approval to market medicinal products in the USA and Europe. The legal framework and the roles of major players in regulation are presented. The life-cycle of a drug is outlined. The various procedures available for assessment and approval of products are described and their requirements outlined. Obligations to be fulfilled after marketing approval are discussed.

ESS01: Essentials of EU and US Regulatory Affairs for Human Medicinal Products
Delivered Online On Demand3 hours
£99

8 Japanese Philosophies for CBT - A Practical Introduction

By Practical CBT

CBT Japanese philosophy practical

8 Japanese Philosophies for CBT - A Practical Introduction
Delivered OnlineFlexible Dates
£40

Data Analytics Workflows for Artificial Lift, Production and Facility Engineers

By EnergyEdge - Training for a Sustainable Energy Future

Data Analytics Workflows for Artificial Lift, Production and Facility Engineers
Delivered in Internationally or OnlineFlexible Dates
£2132 to £2480

SUB05: Electronic Common Technical Document (eCTD)

By Zenosis

The eCTD is mandatory for all applications for marketing approval and all subsequent related submissions in the European Economic Area, the USA and Canada. Other countries intend to make its use mandatory. The eCTD specification has been developed to facilitate the global electronic submission, review and lifecycle management of medicinal product dossiers for regulatory applications. It broadens the scope of the CTD to include information on variations, renewals and amendments, so that it is no longer a static document but is updatable throughout the life of the product. This module outlines the eCTD specification, discusses the approach to regional differences in dossiers, and provides guidance on creation of an eCTD submission. The module provides a training and reference tool that will be of particular value to those new to the use of the format.

SUB05: Electronic Common Technical Document (eCTD)
Delivered Online On Demand2 hours 30 minutes
£126

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

Advanced Heat Exchanger Design, Performance, Inspection, Maintenance and Operation

By EnergyEdge - Training for a Sustainable Energy Future

Boost your expertise in heat exchanger design, performance, inspection, maintenance, and operation with Energyedge's advanced classroom training. Enroll now!

Advanced Heat Exchanger Design, Performance, Inspection, Maintenance and Operation
Delivered In-PersonWed, May 2800:30
£2399 to £2599

ICT01: Compliance with Regulation 21 CFR Part 11 on Electronic Records and Electronic Signatures

By Zenosis

21CFR11 applies to records that are required to be submitted to the FDA, or that are subject to FDA inspection, and that are in electronic form – that is, as computer files. It applies to all computer systems used to create, modify, maintain, archive, retrieve, or transmit such records – from a humble spreadsheet program to a complex information management system.

ICT01: Compliance with Regulation 21 CFR Part 11 on Electronic Records and Electronic Signatures
Delivered Online On Demand1 hour 30 minutes
£74

Upstream Petroleum Economics, Risk and Fiscal Analysis

By EnergyEdge - Training for a Sustainable Energy Future

Upstream Petroleum Economics, Risk and Fiscal Analysis
Delivered in Internationally or OnlineFlexible Dates
£2751 to £3199
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