validation refers to establishing documented evidence that a process or system, when operated within established parameters, can perform effectively and reproducibly to produce a medicinal product meeting its pre-determined specifications and quality attributes
Monday, January 1, 2018
Principles Risk Based Process Safety applied to ICH-Q9 "Risk Assessment"
Protecting people’s lives by reducing incidents drastically. Website: http://ift.tt/2DMEwPD Youtube channel: https://www.youtube.com/channel/UCsrjy36NHLKv6ShF30RwLjg Brantford, Ontario: http://ift.tt/2EtMb6l More information about process safety management: http://ift.tt/2DLCsak I have worked with major companies in the pharmaceutical, chemical, food and manufacturing industries. Process Safety Management: I have helped organizations to implement and coordinate elements of the process safety management program to prevent outcomes such as fires, explosions or releases to protect the environment and public safety. Health and Safety I have helped companies to develop and implement health and safety programs and strategies to achieve legal compliance and incident reduction locally and internationally. Safety Engineering. I have helped operations to reach safety compliance in various stages of production, starts up operations, and equipment acquisition to comply with safety regulations, codes and standards to prevent the incident and protect employees. Call me today 613-464-0562 to help you to identify all possible hazards of your operations. You can also check PHARMA-CHEMICALSAFETY pages at: Youtube: https://www.youtube.com/channel/UCsrjy36NHLKv6ShF30RwLjg Facebook: http://ift.tt/2EyQI7I Twitter: https://www.twitter.com/Pharmachemical1 LinkedIn: http://ift.tt/2DLU4mr Google+: http://ift.tt/2EwfBRt
Subscribe to:
Post Comments (Atom)
Pharmaceutical Validation Documentation Requirements
Pharmaceutical validation is a critical process that ensures that pharmaceutical products meet the desired quality standards and are safe fo...
-
K. Dashora, D. Singh, Swarnlata Saraf and S. Saraf *. Institute of Pharmacy, Pt.RavishankarShuklaUniversity, Raipur 492 010. *Author for ...
-
Validation of the Autoclave is classified into the following 1.0 OQ – Operational Qualification 2.0 PQ – Performance Qualification The valid...
-
Cold storage is a relatively simple cold room that is commonly used to store material between 2[degrees] to 8[degrees]C. Such cold rooms a...
No comments:
Post a Comment