Welcome, Guest

Pharmaceutical

Title Publisher Training Time Price
An Introduction to Clinical Trial Preparation and Design (CT04) Zenosis 4 Hours £ 200.00
An Introduction to Clinical Trials and Drug Development (CT07) Zenosis 1 Hour 30 Minutes £ 74.00
An Introduction to Drug Safety and Pharmacovigilance (PV03) Zenosis 2 Hours £ 99.00
An Introduction to Good Manufacturing Practice for Medicinal Products (GMP01) Zenosis 1 Hour 30 Minutes £ 74.00
An Introduction to Pharmacokinetics and Pharmacodynamics in Drug Development and Registration (PKPD01) Zenosis 1 Hour 30 Minutes £ 74.00
Clinical Trial Monitoring: Site Evaluation and Set-up (CT06) Zenosis 1 Hour 30 Minutes £ 74.00
Clinical Trial Monitoring: Study Monitoring, Documentation and Closure (CT08) Zenosis 2 Hours £ 99.00
Clinical Trial Safety Reporting Requirements in the EU and USA (CT14) Zenosis 2 Hours £ 99.00
Commissioning and Installation Qualification (VAL03) Zenosis 1 Hour 30 Minutes £ 99.00
Compliance with Regulation 21 CFR Part 11 on Electronic Records and Electronic Signatures (ICT01) Zenosis 1 Hour 30 Minutes £ 74.00
Computer Systems Validation, Part 1: Planning (VAL06) Zenosis 1 Hour £ 99.00
Computer Systems Validation, Part 2: Implementation (VAL07) Zenosis 1 Hour £ 99.00
Conducting Pharmacokinetic and Pharmacodynamic Studies (PKPD02) Zenosis 1 Hour 30 Minutes £ 74.00
Consumer-directed Advertising and Online Promotion of Prescription Drugs in the USA (SAM03) Zenosis 1 Hour £ 99.00
Electronic Common Technical Document (eCTD) (SUB05) Zenosis 2 Hours 30 Minutes £ 120.00
Equipment Cleaning Validation (VAL05) Zenosis 1 Hour 30 Minutes £ 99.00
Essentials of EU and US Regulatory Affairs for Human Medicinal Products (ESS01) Zenosis 3 Hours £ 149.00
Good Clinical Practice Inspections and Audits (CT09) Zenosis 2 Hours 30 Minutes £ 120.00
Good Manufacturing Practice for the Warehouse (GMP04) Zenosis 1 Hour 30 Minutes £ 74.00
Good Practices (GxP) in Drug Development and Manufacturing (GXP01) Zenosis 30 Minutes £ 29.00
How to Conduct Clinical Research Under the EU Clinical Trials Regulation (CT12) Zenosis 1 Hour £ 49.00
How to Gain Approval to Conduct Clinical Trials in Europe (CT01) Zenosis 3 Hours £ 149.00
How to Gain Approval to Market a Generic Drug in the USA (SUB13) Zenosis 3 Hours £ 149.00
How to Gain Authorisation for Clinical Research under the EU Clinical Trials Regulation (CT11) Zenosis 2 Hours £ 99.00
ICH Good Clinical Practice (CT03) Zenosis 3 Hours £ 149.00
Introduction to Validation (VAL01) Zenosis 1 Hour 30 Minutes £ 99.00
Legal and Regulatory Framework for Advertising and Promotion of Prescription Drugs in the USA (SAM01) Zenosis 1 Hour £ 99.00
Marketing of Prescription Drugs in the USA - Interactions with Healthcare Professionals (SAM04) Zenosis 1 Hour £ 99.00
Medical Devices - An Introduction to the Regulation of Medical Devices (MD01) Zenosis 1 Hour £ 49.00
Operational and Performance Qualification (VAL04) Zenosis 1 Hour £ 99.00
Orphan Drug Designation in the USA and Europe (SUB01) Zenosis 1 Hour 30 Minutes £ 74.00
Preparing Submissions in the Common Technical Document (CTD) Format (SUB04) Zenosis 1 Hour 30 Minutes £ 74.00
Registration of Medicinal Products Based on Monoclonal Antibodies (SUB12) Zenosis 1 Hour 30 Minutes £ 74.00
Regulatory Requirements and Guidance on Advertising and Promotion of Prescription Drugs in the USA (SAM02) Zenosis 1 Hour 30 Minutes £ 99.00
Risk Management Planning for Medicinal Products (PV05) Zenosis 1 Hour 30 Minutes £ 61.00
Safety Reporting in Clinical Trials (CT13) Zenosis 2 Hours £ 99.00
Signal Detection and Management in Pharmacovigilance (PV04) Zenosis 1 Hour 30 Minutes £ 74.00
The Decentralised Procedure (DCP) (SUB11) Zenosis 2 Hours £ 99.00
The European Centralised Procedure (CP) (SUB02) Zenosis 1 Hour 30 Minutes £ 74.00
The Investigational New Drug Application (IND) to Conduct FDA-regulated Clinical Trials (CT10) Zenosis 3 Hours £ 149.00
The Mutual Recognition Procedure (MRP) (SUB03) Zenosis 2 Hours £ 99.00
The New Drug Application (NDA) for Marketing Approval in the USA (SUB09) Zenosis 3 Hours 30 Minutes £ 176.00
The Regulatory Pathway to Licensure of Follow-on Biologics (Biosimilars) in the USA (SUB14) Zenosis 30 Minutes £ 29.00
Validation Plans and Documentation (VAL02) Zenosis 1 Hour 30 Minutes £ 99.00
Variations to Marketing Authorisations in Europe (SUB06) Zenosis 3 Hours 30 Minutes £ 176.00