CIS Makes Catching Up with Supplier Audits Easier with Free Program Assessment for Pharma Manufacturers
Philadelphia, PA, December 08, 2010 --(PR.com)-- Compliance Implementation Services (CIS), a pharmaceutical compliance consulting firm, announced today that it will offer a free supplier management program assessment to pharmaceutical manufacturers in an effort to assist them with their 2010-2011 supplier audits.
“As a former Director of Quality for a major pharmaceutical manufacturer, I remember how frustrating it was to try to catch up with supplier audits and have to send my best people out of the plant when they were needed the most,” said Venessa Piper-Givler, Director of Global Manufacturing for CIS. “The certified and experienced auditing team at CIS can help alleviate that frustration by offering a free assessment that will help manufacturers get the ‘big picture’ of their supplier management program.”
The CIS offer includes a free on-site, two-day assessment —a $2000 value — of a U.S.-based company’s supplier management program performed by an American Society for Quality-certified auditor. The promotion includes a full post-audit report compiled by auditors with an extensive background in final dosage, API, raw materials, and sterile drug product manufacturing.
To schedule a free supplier management program assessment, send an email to info@cis-partners.com.
About CIS
Compliance Implementation Services (CIS) is a consulting firm specializing in compliance strategies for the pharmaceutical industry, from Global Clinical Research and Development, through Manufacturing, U.S. Commercial Compliance, and Government Programs. Founded in 2004, CIS provides its clients with a deep understanding of industry laws and regulations, innovative and practical applications, and custom solutions to establish a “Culture of Compliance” that is both meaningful and sustainable.
CIS experts identify, assess and prioritize an organization’s exposure to compliance risks, subsequently developing and implementing risk evaluation and mitigation techniques to ensure adherence to legal and regulatory requirements. For more information, visit www.cis-partners.com.
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“As a former Director of Quality for a major pharmaceutical manufacturer, I remember how frustrating it was to try to catch up with supplier audits and have to send my best people out of the plant when they were needed the most,” said Venessa Piper-Givler, Director of Global Manufacturing for CIS. “The certified and experienced auditing team at CIS can help alleviate that frustration by offering a free assessment that will help manufacturers get the ‘big picture’ of their supplier management program.”
The CIS offer includes a free on-site, two-day assessment —a $2000 value — of a U.S.-based company’s supplier management program performed by an American Society for Quality-certified auditor. The promotion includes a full post-audit report compiled by auditors with an extensive background in final dosage, API, raw materials, and sterile drug product manufacturing.
To schedule a free supplier management program assessment, send an email to info@cis-partners.com.
About CIS
Compliance Implementation Services (CIS) is a consulting firm specializing in compliance strategies for the pharmaceutical industry, from Global Clinical Research and Development, through Manufacturing, U.S. Commercial Compliance, and Government Programs. Founded in 2004, CIS provides its clients with a deep understanding of industry laws and regulations, innovative and practical applications, and custom solutions to establish a “Culture of Compliance” that is both meaningful and sustainable.
CIS experts identify, assess and prioritize an organization’s exposure to compliance risks, subsequently developing and implementing risk evaluation and mitigation techniques to ensure adherence to legal and regulatory requirements. For more information, visit www.cis-partners.com.
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Contact
Compliance Implementation Services
Marni Schribman
484-445-7255
www.cis-partners.com
Marni Schribman
484-445-7255
www.cis-partners.com
Contact
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