Validating pharmaceutical teen dating violence awareness national
Within the scope of this document Risk Analysis is performed.
The next thing to consider when planning the process of qualification and validation is the importance of cooperation of several different specialists: technologists, engineers, metrologists, and others.
They measure and analyze the process, audit and calibrate equipment and create a document trail that shows the process leads to a consistent result to ensure the highest quality products are produced.
For investigations of failures or action levels, a specific method is usually preferable.
As a factor directly affecting the production of high quality medicines, validation will always remain one of the essential indicators of quality and efficiency of production.
We provide comprehensive validation services for manufacturers and distributors of pharmaceutical, biotechnological and veterinary products, manufacturers of pharmaceutical, biotechnological and medical equipment, laboratories, health care institutions, food producers, manufacturers of electronic components. The guiding document on qualification and validation of the object is the Validation Master Plan.
The products made must be exactly the same every time and are tested at the end of the production process to ensure that this is the case but final end product testing isn’t enough.
In addition, the processes, systems and equipment that lead to their manufacture are closely scrutinised too.