Pharmaceutical

Title Publisher Training Time Base Price
An Introduction to Clinical Trial Preparation and Design Zenosis 4 Hours £ 200.00
An Introduction to Clinical Trials and Drug Development Zenosis 1 Hour 30 Minutes £ 74.00
An Introduction to Drug Safety and Pharmacovigilance Zenosis 2 Hours £ 98.00
An Introduction to Good Manufacturing Practice for Medicinal Products Zenosis 1 Hour 30 Minutes £ 74.00
An Introduction to Pharmacokinetics and Pharmacodynamics in Drug Development and Registration Zenosis 1 Hour 30 Minutes £ 74.00
Clinical Trial Monitoring: Site Evaluation and Set-up Zenosis 1 Hour 30 Minutes £ 74.00
Clinical Trial Monitoring: Study Monitoring, Documentation and Closure Zenosis 2 Hours £ 98.00
Commissioning and Installation Qualification Zenosis 1 Hour 30 Minutes £ 120.00
Compliance with Regulation 21 CFR Part 11 on Electronic Records and Electronic Signatures Zenosis 1 Hour 30 Minutes £ 74.00
Computer Systems Validation, Part 1: Planning Zenosis 1 Hour £ 120.00
Computer Systems Validation, Part 2: Implementation Zenosis 1 Hour £ 120.00
Conducting Pharmacokinetic and Pharmacodynamic Studies Zenosis 1 Hour 30 Minutes £ 74.00
Corrective and Preventive Action (CAPA) in Medicinal Products Manufacture Zenosis 1 Hour £ 39.00
Electronic Common Technical Document (eCTD) Zenosis 2 Hours 30 Minutes £ 120.00
Equipment Cleaning Validation Zenosis 1 Hour 30 Minutes £ 120.00
Essentials of EU and US Regulatory Affairs for Human Medicinal Products Zenosis 3 Hours £ 149.00
Essentials of Monoclonal Antibodies Zenosis 1 Hour £ 39.00
Good Clinical Practice Inspections and Audits Zenosis 2 Hours 30 Minutes £ 120.00
Good Documentation Practice Zenosis 1 Hour £ 39.00
Good Manufacturing Practice for the Warehouse Zenosis 1 Hour 30 Minutes £ 74.00
Good Manufacturing Practice in Cleaning and Sanitation Zenosis 1 Hour £ 39.00
Good Manufacturing Practice in Packaging Medicinal Products Zenosis 1 Hour £ 39.00
Good Manufacturing Practice in Processing Medicinal Products Zenosis 1 Hour £ 39.00
Good Pharmacoepidemiology Practice Zenosis 1 Hour £ 39.00
How to Gain Approval to Conduct Clinical Trials in Europe Zenosis 3 Hours £ 149.00
How to Gain Approval to Market a Generic Drug in the USA Zenosis 3 Hours £ 149.00
ICH Good Clinical Practice Zenosis 3 Hours £ 149.00
Introduction to Validation Zenosis 1 Hour 30 Minutes £ 120.00
Medical Devices - An Introduction to the Regulation of Medical Devices Zenosis 1 Hour £ 49.00
Operational and Performance Qualification Zenosis 1 Hour £ 120.00
Orphan Drug Designation in the USA and Europe Zenosis 1 Hour 30 Minutes £ 74.00
Preparing Submissions in the Common Technical Document (CTD) Format Zenosis 1 Hour 30 Minutes £ 74.00
Registration of Medicinal Products Based on Monoclonal Antibodies Zenosis 1 Hour 30 Minutes £ 74.00
Risk Management Planning for Medicinal Products Zenosis 1 Hour 30 Minutes £ 61.00
Signal Detection and Management in Pharmacovigilance Zenosis 1 Hour 30 Minutes £ 74.00
The Decentralised Procedure (DCP) Zenosis 2 Hours £ 98.00
The European Centralised Procedure (CP) Zenosis 1 Hour 30 Minutes £ 74.00
The Investigational New Drug Application (IND) to Conduct FDA-regulated Clinical Trials Zenosis 3 Hours £ 149.00
The Mutual Recognition Procedure (MRP) Zenosis 2 Hours £ 98.00
The New Drug Application (NDA) for Marketing Approval in the USA Zenosis 3 Hours 30 Minutes £ 176.00
The Regulatory Pathway to Licensure of Follow-on Biologics (Biosimilars) in the USA Zenosis 30 Minutes £ 25.00
Urgent Safety Restrictions Zenosis 45 Minutes £ 39.00
Validation Plans and Documentation Zenosis 1 Hour 30 Minutes £ 120.00
Variations to Marketing Authorisations in Europe Zenosis 3 Hours 30 Minutes £ 176.00

Contact Us

Unit G1 Hoxton Works, 128 Hoxton Street, London, N1 6SH, England
Phone: +44 (0)20 7613 3444

Follow Us