Mon premier blog

Good Design Practices for GMP Pharmaceutical Facilities Andrew Signore, Terry Jacobs
Publisher: Informa Healthcare

Ensure all activities are in compliance with company policies, good engineering practices and GMP standards. Distribution Center Facility Manager – GMP: Pharmaceutical /medical device. Thorough, well written, detailed, and interesting…a good reference for many in the Pharmaceutical industry…--Drug Development and Industrial Pharmacy…immensely informative, rich in detail, and well-indexed…. Posted on May 19, 2013 by Ron Dowdy medical device companies throughout the USA. My client is in urgent need of a Process Engineer to work on projects for major clients. Prepare and maintain departmental budget; Assist with planning, design, implementation, communication, and delivery of company's logistics initiatives. My client is an international contractor who specialises in the pharmaceutical industry. These guidelines focus primarily on the design and good manufacturing practices (GMP) requirements for HVAC systems for pharmaceutical facilities. You will be working on a variety of process packages for which Work on process packages for Pharmaceutical projects which include both primary and secondary facilities. FDA and other regulatory body requirements are discussed and the reasoning behind them. The warehouse includes cold storage and must remain FDA compliant requiring adherence to current Good Manufacturing Practices (GMP). This course explores some of the best practices of pharmaceutical facility design with an emphasis on the regulatory aspect.