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Booklets

A Monitor’s Guide to Investigator Site Audits Booklet

A Practical Guide for the Good Laboratory Practice Study Director

A Practical Guide to GLP Quality Assurance Booklet

A Practical Guide to GLP in the Analytical Laboratory Booklet

Auditing Computerised Systems Booklet

CAPA: Effective approaches to improvement

Comparison of Pharmacovigilance Regulations in Europe and Japan

Computerised System Validation Booklet

Electronic Standard Operating Procedures Booklet

Good Clinical Laboratory Practice Booklet

Good Clinical Practice Regulatory Authority Inspections Booklet

Guide to the Role and Responsibilities of GLP Management Booklet

Guidelines for Quality in Non-Regulated Scientific Research Booklet

Hosting an External GLP Inspection Booklet

Investigators Guide to Investigator Site Audits Booklet

Management Review 2018 Booklet

Management of the Training and Competency of Personnel in GxP and Research Environments

Medical Devices Regulation Booklet

Pharmacovigilance Agreements (PVAs): Guidance on the Quality Oversight and Operational Aspects

Pharmacovigilance Auditing Booklet

Quality Assurance in Pharmaceutical Due Diligence Booklet

Quality Risk Management Booklet

Quality Systems Guide

Quality in Research Booklet

RQA Employment Survey Full Report 2017

RQA Employment Survey Summary Report 2017

The FMEA Toolkit

The Role of QA in Outsourcing Booklet

The Role of the Monitor in Veterinary Clinical Studies Booklet

Virtual Event Platform