Standard Operating Procedure (SOP) and Standard Test Method (STM) Requirements

Who Should Attend
This webinar will provide a great resource to Pharmaceutical, Biotechnology, Biologics, Drugs, Medical Device, In-vitro Diagnostics Industry personnel within the following functions:Quality Control, Quality Assurance, Microbiologist, Chemist, Analysts, Manufacturing, Validation, Facilities, Materials, Engineering, Vendors/Suppliers, all Technical Writers and SOP/STM Users, Regulatory Affairs and all levels of management.

Description
This course will be available On Demand: August 2, 2013

Designing an effective Standard Operating Procedure (SOP) and Standard Test Method (STM) is the pre-requisite to complying with the different regulations guiding the manufacturing and testing of products. A well-established procedure and test method improves the numbers of manufacturing, testing and personnel deviations which indirectly affects the quality and life cycle process of a manufactured product.

This 90-minute accredited training course will provide the attendee the ability to understand the sequence of designing, development, drafting, processing and approval of an effective and compliant SOP or STM. The industry applications, regulations, content, organization, development, management process/cycle, content and formatting of an SOP and STM will be discussed. Understanding these requirements will aid in the reduction of manufacturing and testing errors arising from an unclear, poorly planned/executed and vague procedures that are left to several varying interpretations and applications which may sometimes lead to non-compliance.