Pharmaceutical Process and Cleaning Validation
Services Available Nationwide
Our service for process validation ensures that the processes set in place by your company consistently produce the desired outcomes – rendering products that meet requirements on quality and specification. This could include the analysis of manufacturing, packaging and sterilisation processes within the pharmaceutical industry.
Our pharmaceutical validation services can be broken down into three sections:
+ Process Design
Our team will work with you to develop an understanding of the desired outcomes of the process in question, before developing said process, along with a strategy to ensure process control throughout.
+ Process Qualification
The process we have designed will then undergo thorough evaluation to ensure that the required outcomes are being met. We will also evaluate the ongoing reliability of the process as it pertains to efficient commercial manufacturing. We'll repair a final report and take measures to ameliorate any imperfect elements.
+ Continued Process Verification
As routine production is carried out, ongoing verification will be performed, to ensure that the process is stable. We will undertake periodic assessments of the process also, to identify and undertake necessary alterations or recalibration of the process.
Thanks to the expertise of our experienced staff, we can construct and execute master plans for cleaning development and cleaning validation. We begin with a hazard identification process and examine cleaning processes in-depth, to ensure that all potential hazards are identified and mitigated before they have the chance to exacerbate. This includes chemical and microbiological hazards, as well as API, cleaning agents and Micro/Endotoxins usage in your workplace.
Controlled Processes, Developed in Accordance with Experts
Get in contact with your dedicated team and begin refining your processes today.