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Hallam Pharma Consulting Ltd | Quality Assurance * GCP Audit * Training * Medical Writing

Quality Assurance * GCP Audit * Training * Medical Writing (by Shirley Hallam)

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Hallam Pharma Consulting

Shirley Hallam

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Pete●●●●ough , Cambridgeshire, PE4 6NL

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Hallam Pharma Consulting

Shirley Hallam

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Pete●●●●ough , Cambridgeshire, PE4 6NL

GB

44.1●●●●1782
sh●●●●●●●●●●●●@aol.com

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Hallam Pharma Consulting Ltd | Quality Assurance * GCP Audit * Training * Medical Writing | gcp-quality.com Reviews
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Quality Assurance * GCP Audit * Training * Medical Writing (by Shirley Hallam)
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Hallam Pharma Consulting Ltd | Quality Assurance * GCP Audit * Training * Medical Writing | gcp-quality.com Reviews

https://gcp-quality.com

Quality Assurance * GCP Audit * Training * Medical Writing (by Shirley Hallam)

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1

FDA publishes guidance on Electronic Data Capture in eCRFs | Hallam Pharma Consulting Ltd

http://gcp-quality.com/2013/10/24/fda-publishes-edc-guidance

Hallam Pharma Consulting Ltd. Quality Assurance * GCP Audit * Training * Medical Writing. Training and Other Services. FDA publishes guidance on Electronic Data Capture in eCRFs. Posted by Shirley Hallam in Quality Management. The United States Food and Drugs Administration (FDA) has published new guidance on the use of electronic data capture in clinical trials. Identification and specification of authorized source data originators. Use and description of computerized systems in clinical investigations.

2

Ethics | Hallam Pharma Consulting Ltd

http://gcp-quality.com/tag/ethics

Hallam Pharma Consulting Ltd. Quality Assurance * GCP Audit * Training * Medical Writing. Training and Other Services. An Introduction to Good Clinical Practice. Posted by Shirley Hallam in Approvals. New Readers Start Here. For research involving medication or medical devices, GCP is underpinned by European and UK legislation. For other research involving NHS patients, GCP provides a helpful framework for researchers to consider in designing projects with arrangements that are proportionate to risk,...

3

MHRA | Hallam Pharma Consulting Ltd

http://gcp-quality.com/tag/mhra

Hallam Pharma Consulting Ltd. Quality Assurance * GCP Audit * Training * Medical Writing. Training and Other Services. An Introduction to Good Clinical Practice. Posted by Shirley Hallam in Approvals. New Readers Start Here. For research involving medication or medical devices, GCP is underpinned by European and UK legislation. For other research involving NHS patients, GCP provides a helpful framework for researchers to consider in designing projects with arrangements that are proportionate to risk,...

4

GCP | Hallam Pharma Consulting Ltd

http://gcp-quality.com/tag/gcp

Hallam Pharma Consulting Ltd. Quality Assurance * GCP Audit * Training * Medical Writing. Training and Other Services. EU Clinical Trials Regulation. Posted by Shirley Hallam in Approvals. The European Union Clinical Trials Regulation 536/2014. Was published in the official EU Journal on 27th May 2014. It will enter into force on 16th June 2014, and will be implemented either from 28th May 2016, or six months after the necessary portal and databases become fully functional, whichever is the later. Good C...

5

Quality Assurance | Hallam Pharma Consulting Ltd

http://gcp-quality.com/quality-assurance

Hallam Pharma Consulting Ltd. Quality Assurance * GCP Audit * Training * Medical Writing. Training and Other Services. Hallam Pharma Consulting combines in-depth knowledge of regulatory requirements with practical experience of conducting clinical research. We work with our clients to produce customised services which meet the needs of their organisations. Preparation of harmonised comprehensive clinical Standard Operating Procedures (SOPs) for a recently merged international pharmaceutical company.

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Hallam Pharma Consulting Ltd | Quality Assurance * GCP Audit * Training * Medical Writing

Hallam Pharma Consulting Ltd. Quality Assurance * GCP Audit * Training * Medical Writing. Training and Other Services. EU Clinical Trials Regulation. Posted by Shirley Hallam in Approvals. The European Union Clinical Trials Regulation 536/2014. Was published in the official EU Journal on 27th May 2014. It will enter into force on 16th June 2014, and will be implemented either from 28th May 2016, or six months after the necessary portal and databases become fully functional, whichever is the later. Good C...

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