Sherwood International Consulting Group Facilitating Regulatory Compliance Worldwide...
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Audits

Compliance to current regulations and guidelines is critical. Non-compliance can result in delay to market, negative market perception, and costly corrective actions diverting resources or resulting in product recall.

Let us help you assess the Adequacy and Effectiveness of your Quality Systems. Our auditing methodology ensures your risk management is effective.

For companies conducting clinical studies, let us help you ensure your studies meet GCP requirements.

  

Too often auditors may highlight issues that are perceived to be major, but in reality, are minor issues. By applying risk management to audit observations, we can help distinguish if there is risk to product safety, regulatory compliance issues or even an element which may be compliant but has the potential to become non-compliant if preventive action is not taken.

In keeping with the identification of Risk associated with an audit finding, we can also help you discover multiple options on how to resolve the finding. In today’s business, risk management and flexibility are key to an expeditious feedback system that promotes productivity rather than tax productivity.

Types of audits we conduct include:

  • GMP / ISO
  • Internal/External
  • Mock FDA
  • Due Diligence (Acquisitions)
  • Remote Supplier
  • Clinical Study
  • Vendor Qualification
  • Electronic Data Systems
  • Clinical Study Site Qualification
  • IRB

 

Please contact us for further information.

Download our Audit information in PDF format.

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Sherwood International Consulting Group • 5385 Hollister Ave. Box 209 • Santa Barbara, CA 93111 • Tel: 805-708-6442
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