This course covers the key concepts of GxP computerised systems validation and compliance, including the key regulatory requirements and effective industry good practice based on GAMP®5.

Computerised systems validation and compliance is a basic GxP regulatory requirement. Inadequate or inappropriate validation approaches can lead to serious compliance and quality problems. Compliant and validated computerized systems are a prerequisite for effective Data Integrity

This course describes a practical and efficient framework for computerised systems validation and compliance, following current industry good practice, and gives attendees an appreciation of how these ideas may be applied to their own systems and processes.

Pharmaceutical validation professionals, IT, Engineering, Quality Assurance, Qualified Persons, Quality Control and Project Managers in the GxP and validation area.

The course is also relevant for any IT or related service providers (including cloud providers), and providers of software products, or computerized systems and equipment to life science companies.

PROGRAMME

The course covers the following topics:Regulatory environment and risk-based approaches

Current regulatory expectations for GxP computerized systems

EU GMP Annex 11 requirements for computerised systems

Overview of current industry good practice based on GAMP®5

Computerised system lifecycle approach

Validation planning and reporting

Regulated Company and Supplier Responsibilities

Application to Cloud Computing and Cloud Service Providers

Quality Risk Management (QRM) approach

Testing of GxP Systems

Operation of GxP Systems

Impact on Data Integrity

Application of ideas and concepts to your systems