Product category:
Laboratory and scientific consultancy services
News Release from: Smarttech Consulting Services | Subject: Step Process
Edited by the Laboratorytalk Editorial
Team on 23 May 2005
Business improvements for pharma
processes
Consultancy will provide businesses with a formula to create improvements utilising technology for enabling regulatory compliance
Smarttech Consulting Services, a provider of consultancy within the pharmaceutical industry, announces the release of the Step Process which, it says, will provide businesses with a consultative formula to create improvements utilising technology for enabling regulatory compliance "Companies that operate in regulated environments such as MHRA, FDA, US SEC or ISO are looking for a better business return when investing in technology
This article was originally published on Laboratorytalk on 19 Apr 2006 at 8.00am (UK)
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"We have the experience help within our services for regulated industries" said Adrian Carter, director.
"We have adopted a flexible methodology, Step Process, which is based on investigation and understanding our clients' needs and action orientated results aimed towards the implementation of the business benefits identified".
Using on site team workshops, one on one consultation, or remote multimedia training for life science business managers, end users, and suppliers to the regulated industries, SmarttechCS says it can extract specific advantages to their business aims.
"Companies should be able to deploy a regulatory remediation solution within their existing process or laboratory environment without excessive costs.
"As compliance regulations become standardised worldwide, more companies are looking for assistance to provide a measurable business return for their investment" said Trevor Swift, director for Smarttech CS.
"We are able to use our experience in helping businesses in the use of technology to aid project management, electronic document management (eDMS), corrective actions and preventive actions (Capa) systems, electronic laboratory note books (ELN) or laboratory information management systems (Lims) and instrument interfacing, when used for regulatory compliance such as FDA 21 CFR part11 and Section 404 of the Sarbanes-Oxley Act (Sox404)".
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