4.2 Validation documentation should include change control records (if applicable) and reports on any deviations observed during the validation process. 4.3 An up to date listing of all relevant systems and their GMP functionality (inventory) should be available. Validation of Laboratory Instruments. Marko N a rhi, Helsinki University of Technology, Helsinki, Finland, National GMP Regulations and Codes and International GMP Guides and Guidelines: Corre-spondences and Differences. Kenneth J. Nolan, Nolan & Auerbach, Fort Lauderdale Florida,, Enforcement of Good Manufacturing Practices Good manufacturing practice guidelines provide guidance for manufacturing, testing, and quality assurance in order to ensure that a manufactured product is safe for human consumption or use. Many countries have legislated that manufacturers follow GMP procedures and create their own GMP guidelines that correspond with their legislation. Reservation Form (Please complete in full) F SAP - Validation and GMP Compliance, 6-7 November 2018, Berlin, Germany F Virtual IT Systems in a GxP Environment, 8-9 November 2018, Berlin, Germany * Mr * Ms Title, first name, surname Company Department Important: Please indicate your company's VAT ID Number P.O. Number (if applicable) For more information about GMP guidelines and to find out how our software can help your company meet current good manufacturing practices, contact a MasterControl representative at 801-942-4000 or visit MasterControl's Resource Center for free white papers, webinars, and other informative downloads. Health Canada resources on good manufacturing practices (GMP) for drugs and health products. Cleaning Validation Guidance (GUI-0028) [2011-12-16] Request for an Inspection of a Foreign Site Form (FRM-0213) Good Manufacturing Practices - Foreign Site Inspection Services Agreement Form Risk-Based Validation and Requalification of Processes & Equipment Nancy Tomoney -Pharmaceutical GMP related validation -Guid