Principles and Audit Planning Planning and preparation Internal audits are critical element of your quality management system. Your approach must be both systematic and documented to remain compliant Information from an internal audit provides management with the knowledge they need to show how effectively the company maintains the quality of the product and their processes Audit types and techniques Establishing an audit program for suppliers, contractors and company sites Internal vs. external audits The audit processes

Date : 27th July 2017 to 28th July 2017

Place : United States, Philadelphia, pa

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900972SEMINAR?allconferencealerts_july_2017_SEO

Contact Person:Eevnt Manager

Description:

Principles and Audit Planning Planning and preparation Internal audits are critical element of your quality management system. Your approach must be both systematic and documented to remain compliant Information from an internal audit provides management with the knowledge they need to show how effectively the company maintains the quality of the product and their processes Audit types and techniques Establishing an audit program for suppliers, contractors and company sites Internal vs. external audits The audit processes

Principles and Audit Planning Planning and preparation Internal audits are critical element of your quality management system. Your approach must be both systematic and documented to remain compliant Information from an internal audit provides management with the knowledge they need to show how effectively the company maintains the quality of the product and their processes Audit types and techniques Establishing an audit program for suppliers, contractors and company sites Internal vs. external audits The audit processes will be held in Philadelphia, pa,United States on date 2017-07-28

---

Deadline for abstracts/proposals : 26th July 2017

Keynote Speakers : David R. Dills, Global Regulatory Affairs & Compliance Consultant currently provides regulatory affairs and compliance consultative services for early-stage and established Class I/II/III device, IVD, biopharmaceutical, cosmetics and nutraceutical manufacturers on the global landscape, and has an accomplished record with more than 27 years of experience in the areas of Regulatory Affairs, Compliance and Quality Systems. He has been previously employed, with increasing responsibilities by dev

Conference Highlights :Clinical Research Associates Clinical Project Managers Regulatory Affairs Professionals Clinical Investigators and Clinical Research Regulatory Affairs Management Regulatory Affairs Specialists Regulatory Project Leads/SME's QA Auditors Supplier Auditors GxP Auditors Compliance Specialists Clinical Affairs Quality Manager Quality Assurance Production/Operations Consultants

Venue :Philadelphia, PA, United States

Check the event website for more details.