Zenosis ®

About us

Zenosis ® offers a unique learning and knowledge transfer solution for the Regulatory affairs and Clinical departments in Pharmaceutical, Biotech, Life Sciences and Clinical Research companies.

Zenosis ® is designed to support companies' drug development lifecycles ensuring compliance is achieved.

All Courses

(49 courses)

Good Practices (GxP) in Drug Development and Manufacturing (GXP01)
by Zenosis ®

£34.80

0 (0)
Clinical Trial Safety Reporting Requirements in the EU and USA (CT14)
by Zenosis ®

£118.80

0 (0)
Safety Reporting in Clinical Trials (CT13)
by Zenosis ®

£118.80

0 (0)
How to Gain Approval to Market a Generic Drug in the USA (SUB13)
by Zenosis ®

£178.80

0 (0)
Variations to Marketing Authorisations in Europe (SUB06)
by Zenosis ®

£211.20

0 (0)
Conducting Pharmacokinetic and Pharmacodynamic Studies (PKPD02)
by Zenosis ®

£88.80

0 (0)
Medical Devices - An Introduction to the Regulation of Medical Devices (MD01)
by Zenosis ®

£58.80

0 (0)
An Introduction to Clinical Trials and Drug Development (CT07)
by Zenosis ®

£88.80

0 (0)
Orphan Drug Designation in the USA and Europe (SUB01)
by Zenosis ®

£88.80

0 (0)
An Introduction to Drug Safety and Pharmacovigilance (PV03)
by Zenosis ®

£118.80

0 (0)
The Regulatory Pathway to Licensure of Follow-on Biologics (Biosimilars) in the USA (SUB14)
by Zenosis ®

£30.00

0 (0)
An Introduction to Pharmacokinetics and Pharmacodynamics in Drug Development and Registration (PKPD01)
by Zenosis ®

£88.80

0 (0)
An Introduction to Clinical Trial Preparation and Design (CT04)
by Zenosis ®

£240.00

0 (0)
The Investigational New Drug Application (IND) to Conduct FDA-regulated Clinical Trials (CT10)
by Zenosis ®

£178.80

0 (0)
The New Drug Application (NDA) for Marketing Approval in the USA (SUB09)
by Zenosis ®

£211.20

0 (0)
Signal Detection and Management in Pharmacovigilance (PV04)
by Zenosis ®

£88.80

0 (0)
Good Clinical Practice Inspections and Audits (CT09)
by Zenosis ®

£144.00

0 (0)
ICH Good Clinical Practice (CT03)
by Zenosis ®

£178.80

0 (0)
Good Documentation Practice (GMP02)
by Zenosis ®

£46.80

0 (0)
An Introduction to Good Manufacturing Practice for Medicinal Products (GMP01)
by Zenosis ®

£88.80

0 (0)
How to Gain Authorisation for Clinical Research under the EU Clinical Trials Regulation (CT11)
by Zenosis ®

£118.80

0 (0)
Marketing of Prescription Drugs in the USA - Interactions with Healthcare Professionals (SAM04)
by Zenosis ®

£118.80

0 (0)
Consumer-directed Advertising and Online Promotion of Prescription Drugs in the USA (SAM03)
by Zenosis ®

£118.80

0 (0)
Regulatory Requirements and Guidance on Advertising and Promotion of Prescription Drugs in the USA (SAM02)
by Zenosis ®

£118.80

0 (0)
Legal and Regulatory Framework for Advertising and Promotion of Prescription Drugs in the USA (SAM01)
by Zenosis ®

£118.80

0 (0)
Registration of Medicinal Products Based on Monoclonal Antibodies (SUB12)
by Zenosis ®

£88.80

0 (0)
Compliance with Regulation 21 CFR Part 11 on Electronic Records and Electronic Signatures (ICT01)
by Zenosis ®

£88.80

0 (0)
The Decentralised Procedure (DCP) (SUB11)
by Zenosis ®

£118.80

0 (0)
Electronic Common Technical Document (eCTD) (SUB05)
by Zenosis ®

£144.00

0 (0)
Clinical Trial Monitoring: Site Evaluation and Set-up (CT06)
by Zenosis ®

£88.80

0 (0)
Preparing Submissions in the Common Technical Document (CTD) Format (SUB04)
by Zenosis ®

£88.80

0 (0)
The Mutual Recognition Procedure (MRP) (SUB03)
by Zenosis ®

£118.80

0 (0)
Clinical Trial Monitoring: Study Monitoring, Documentation and Closure (CT08)
by Zenosis ®

£118.80

0 (0)
The European Centralised Procedure (CP) (SUB02)
by Zenosis ®

£88.80

0 (0)
Good Manufacturing Practice for the Warehouse (GMP04)
by Zenosis ®

£88.80

0 (0)
Corrective and Preventive Action (CAPA) in Medicinal Products Manufacture (GMP07)
by Zenosis ®

£46.80

0 (0)
Good Manufacturing Practice in Cleaning and Sanitation (GMP03)
by Zenosis ®

£46.80

0 (0)
Good Manufacturing Practice in Packaging Medicinal Products (GMP06)
by Zenosis ®

£46.80

0 (0)
Risk Management Planning for Medicinal Products (PV05)
by Zenosis ®

£73.20

0 (0)
Essentials of Monoclonal Antibodies (ESS02)
by Zenosis ®

£46.80

0 (0)
Urgent Safety Restrictions (PV06)
by Zenosis ®

£46.80

0 (0)
Essentials of EU and US Regulatory Affairs for Human Medicinal Products (ESS01)
by Zenosis ®

£178.80

0 (0)
Computer Systems Validation, Part 2: Implementation (VAL07)
by Zenosis ®

£118.80

0 (0)
Computer Systems Validation, Part 1: Planning (VAL06)
by Zenosis ®

£118.80

0 (0)
Equipment Cleaning Validation (VAL05)
by Zenosis ®

£118.80

0 (0)
Operational and Performance Qualification (VAL04)
by Zenosis ®

£118.80

0 (0)
Commissioning and Installation Qualification (VAL03)
by Zenosis ®

£118.80

0 (0)
Validation Plans and Documentation (VAL02)
by Zenosis ®

£118.80

0 (0)
Introduction to Validation (VAL01)
by Zenosis ®

£118.80

0 (0)

Zenosis ®

About us

All Courses

Good Practices (GxP) in Drug Development and Manufacturing (GXP01)

Clinical Trial Safety Reporting Requirements in the EU and USA (CT14)

Safety Reporting in Clinical Trials (CT13)

How to Gain Approval to Market a Generic Drug in the USA (SUB13)

Variations to Marketing Authorisations in Europe (SUB06)

Conducting Pharmacokinetic and Pharmacodynamic Studies (PKPD02)

Medical Devices - An Introduction to the Regulation of Medical Devices (MD01)

An Introduction to Clinical Trials and Drug Development (CT07)

Orphan Drug Designation in the USA and Europe (SUB01)

An Introduction to Drug Safety and Pharmacovigilance (PV03)

The Regulatory Pathway to Licensure of Follow-on Biologics (Biosimilars) in the USA (SUB14)

An Introduction to Pharmacokinetics and Pharmacodynamics in Drug Development and Registration (PKPD01)

An Introduction to Clinical Trial Preparation and Design (CT04)

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

The New Drug Application (NDA) for Marketing Approval in the USA (SUB09)

Signal Detection and Management in Pharmacovigilance (PV04)

Good Clinical Practice Inspections and Audits (CT09)

ICH Good Clinical Practice (CT03)

Good Documentation Practice (GMP02)

An Introduction to Good Manufacturing Practice for Medicinal Products (GMP01)

How to Gain Authorisation for Clinical Research under the EU Clinical Trials Regulation (CT11)

Marketing of Prescription Drugs in the USA - Interactions with Healthcare Professionals (SAM04)

Consumer-directed Advertising and Online Promotion of Prescription Drugs in the USA (SAM03)

Regulatory Requirements and Guidance on Advertising and Promotion of Prescription Drugs in the USA (SAM02)

Legal and Regulatory Framework for Advertising and Promotion of Prescription Drugs in the USA (SAM01)

Registration of Medicinal Products Based on Monoclonal Antibodies (SUB12)

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

The Decentralised Procedure (DCP) (SUB11)

Electronic Common Technical Document (eCTD) (SUB05)

Clinical Trial Monitoring: Site Evaluation and Set-up (CT06)

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

The Mutual Recognition Procedure (MRP) (SUB03)

Clinical Trial Monitoring: Study Monitoring, Documentation and Closure (CT08)

The European Centralised Procedure (CP) (SUB02)

Good Manufacturing Practice for the Warehouse (GMP04)

Corrective and Preventive Action (CAPA) in Medicinal Products Manufacture (GMP07)

Good Manufacturing Practice in Cleaning and Sanitation (GMP03)

Good Manufacturing Practice in Packaging Medicinal Products (GMP06)

Risk Management Planning for Medicinal Products (PV05)

Essentials of Monoclonal Antibodies (ESS02)

Urgent Safety Restrictions (PV06)

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

Computer Systems Validation, Part 2: Implementation (VAL07)

Computer Systems Validation, Part 1: Planning (VAL06)

Equipment Cleaning Validation (VAL05)

Operational and Performance Qualification (VAL04)

Commissioning and Installation Qualification (VAL03)

Validation Plans and Documentation (VAL02)

Introduction to Validation (VAL01)