This is a ‘must to attend’ event for all individuals from industry that are sponsoring and conducting GLP studies in addition to individuals involved in the analysis of human samples from Clinical Trials. The symposium is aimed at Test Facility Management, Quality Assurance, Study Directors, Principal Investigators, Archivists and Scientists. In addition, individuals who provide a consultancy or contract service to facilities, for example, quality assurance consultants or individuals from contract archiving facilities, contract laboratories etc.
Benefits of attending:
Keep up to date with GLP requirements and MHRA expectations regarding conduct of GLP studies and analysis of human samples from Clinical Trials
Recognise the types of compliance issues that test facilities have to deal with on a day to day basis and understand how the regulators address these issues on a case by case basis to maintain acceptable levels of compliance and encouraging innovative and flexible thinking
An opportunity to share concerns and best practice with others
Information provided at the event will help you to implement and develop compliance models that are more effective and efficient
Discover what your peers are doing through managed interactive sessions
Meet the Inspectorate teams and have the opportunity to ask questions on specific aspects affecting your organisation
Understand how the GLPMA (Good Laboratory Practice Monitoring Authority) address complex compliance issues and learn more about the inspectorates approach to risk based inspections
Gain a better understanding of the MHRA program of Clinical Laboratory inspections and learn about common issues identified during clinical laboratory inspections
Discuss current hot topics and be aware of areas of compliance that monitoring authorities are likely to focus on during routine inspections
Delegates attending the MHRA GLP and GCP Laboratories Symposium will be eligible to claim CPD points.
Benefits of attending:
Keep up to date with GLP requirements and MHRA expectations regarding conduct of GLP studies and analysis of human samples from Clinical Trials
Recognise the types of compliance issues that test facilities have to deal with on a day to day basis and understand how the regulators address these issues on a case by case basis to maintain acceptable levels of compliance and encouraging innovative and flexible thinking
An opportunity to share concerns and best practice with others
Information provided at the event will help you to implement and develop compliance models that are more effective and efficient
Discover what your peers are doing through managed interactive sessions
Meet the Inspectorate teams and have the opportunity to ask questions on specific aspects affecting your organisation
Understand how the GLPMA (Good Laboratory Practice Monitoring Authority) address complex compliance issues and learn more about the inspectorates approach to risk based inspections
Gain a better understanding of the MHRA program of Clinical Laboratory inspections and learn about common issues identified during clinical laboratory inspections
Discuss current hot topics and be aware of areas of compliance that monitoring authorities are likely to focus on during routine inspections
Delegates attending the MHRA GLP and GCP Laboratories Symposium will be eligible to claim CPD points.
