Mastering Clinical Trial Documents 2016: Being Ready for Regulation Inspections
SMi’s Mastering Clinical Trial Documents masterclass will take place on the 16th March 2016 in London.
London, United Kingdom, February 17, 2016 --(PR.com)-- Good records management not only has an impact on how effectively an organisation manages its records during the conduct of a clinical study; well-managed clinical study records are critical to demonstrating compliance with GCP and other applicable regulations, as well as supporting regulatory inspections.
In light of the new EU regulation, 5362014, being implemented in May 2016, it is imperative to be up to date with the latest requirements revolving around the documentation of clinical trials.
Through interactive discussions and group activities, this full-day CPD-credited masterclass led by Russell Joyce, Heath Barrowcliff Consulting Ltd., will outline: regulations relating to Trial Master File (TMF), including best practice guidance and the latest thinking from legislators and regulators as well as how clinical study records can be created and managed in both the immediate and long-term to ensure the timely availability of an inspection-ready TMF.
To register visit the event website www.smi-online.co.uk/clinical-documents.asp or contact Matthew Apps on +44 20 7827 6093 or email: mapps@smi-online.co.uk
Benefits of Attending:
• Understand the requirements for clinical study records
• Comprehend how records can be managed more effectively
• Learn how to make best use of clinical study records to enhance information sharing and facilitate more efficient operations
• Improve inspection – readiness to avoid resource-intensive preparations when notified of impending audits and inspections
The masterclass will be hosted by Russell Joyce, Director of Heath Barrowcliff Consulting Ltd. To gain more insight into the masterclass benefits, visit the download section of the event website www.smi-online.co.uk/clinical-documents.asp for an exclusive interview.
There is currently an Early Bird offer saving £50 off the current price which is available until the 29th February 2016.
For more information or to register visit the event website www.smi-online.co.uk/clinical-documents.asp or contact Matthew Apps on +44 20 7827 6093 or email: mapps@smi-online.co.uk
Mastering Clinical Trial Documents Masterclass
16/03/2016
London, UK
SMi Group
Email: zgale@smi-online.co.uk
Phone: Matthew Apps on +44 20 7827 6093
URL: www.smi-online.co.uk/clinical-documents.asp
About SMi Group:
Established since 1993, the SMi Group is a global event-production company that specializes in Business-to-Business Conferences, Workshops, Masterclasses and online Communities. We create and deliver events in the Defence, Security, Energy, Utilities, Finance and Pharmaceutical industries. We pride ourselves on having access to the worlds most forward thinking opinion leaders and visionaries, allowing us to bring our communities together to Learn, Engage, Share and Network. More information can be found at http://www.smi-online.co.uk.
In light of the new EU regulation, 5362014, being implemented in May 2016, it is imperative to be up to date with the latest requirements revolving around the documentation of clinical trials.
Through interactive discussions and group activities, this full-day CPD-credited masterclass led by Russell Joyce, Heath Barrowcliff Consulting Ltd., will outline: regulations relating to Trial Master File (TMF), including best practice guidance and the latest thinking from legislators and regulators as well as how clinical study records can be created and managed in both the immediate and long-term to ensure the timely availability of an inspection-ready TMF.
To register visit the event website www.smi-online.co.uk/clinical-documents.asp or contact Matthew Apps on +44 20 7827 6093 or email: mapps@smi-online.co.uk
Benefits of Attending:
• Understand the requirements for clinical study records
• Comprehend how records can be managed more effectively
• Learn how to make best use of clinical study records to enhance information sharing and facilitate more efficient operations
• Improve inspection – readiness to avoid resource-intensive preparations when notified of impending audits and inspections
The masterclass will be hosted by Russell Joyce, Director of Heath Barrowcliff Consulting Ltd. To gain more insight into the masterclass benefits, visit the download section of the event website www.smi-online.co.uk/clinical-documents.asp for an exclusive interview.
There is currently an Early Bird offer saving £50 off the current price which is available until the 29th February 2016.
For more information or to register visit the event website www.smi-online.co.uk/clinical-documents.asp or contact Matthew Apps on +44 20 7827 6093 or email: mapps@smi-online.co.uk
Mastering Clinical Trial Documents Masterclass
16/03/2016
London, UK
SMi Group
Email: zgale@smi-online.co.uk
Phone: Matthew Apps on +44 20 7827 6093
URL: www.smi-online.co.uk/clinical-documents.asp
About SMi Group:
Established since 1993, the SMi Group is a global event-production company that specializes in Business-to-Business Conferences, Workshops, Masterclasses and online Communities. We create and deliver events in the Defence, Security, Energy, Utilities, Finance and Pharmaceutical industries. We pride ourselves on having access to the worlds most forward thinking opinion leaders and visionaries, allowing us to bring our communities together to Learn, Engage, Share and Network. More information can be found at http://www.smi-online.co.uk.
Contact
SMi Group
Zoe Gale
+44 20 7827 6093
www.smi-online.co.uk/clinical-documents.asp
Zoe Gale
+44 20 7827 6093
www.smi-online.co.uk/clinical-documents.asp
Contact
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