Cleaning of pharmaceutical instruments after a product has been manufactured is critical to ensure that the subsequent products to be manufactured are not contaminated. The removal of the residues of the previous products from manufacturing equipment is known as cleaning. If the whole process of cleaning has been documented, it is referred to as cleaning method validation.
Cleaning validation is proof that the cleaning process is effective to removed all residues of the product that was manufactured, cleaning agents those were used during the cleaning process and prevents micro-organisms from developing. This process is done as a requirement of regulatory authorities.
What is required for a cleaning validation process?
First, you must create a protocol. When preparing a protocol, some of the factors that should be considered are the quality of the water, the detergent to be used, the rinsing period and the system’s size. The protocol should contain the objective of the whole process, the scope of the protocol, responsibilities of the departments, the procedure of cleaning, acceptance criteria and cleaning method validation report.
The people conducting the process should be trained before they start the process of cleaning method validation. They must have knowledge of cleaning procedure, standard operating procedure and validation protocol.
Determine the Parts of the Equipment’s to Clean
There are some parts of the equipment that come into contact with the product during manufacturing. This places should be labeled contact parts while those that do not come into contact with the product are labeled non-contact parts. When cleaning, contact parts of the equipment should be cleaned properly. A lot of care should be taken for cleaning the of the place those are difficult to clean. However, for non-contacts take care that these residues during cleaning do not move to these places. Consideration should still be given to the design of the equipment as this influences how it will be cleaned and the time it takes to clean.
Determine the Detergent Used
A good detergent should be easily removed during the cleaning process by rinsing. Detergents which have residues that are hard to remove usually are discouraged. There before choosing any cleanser, a manufacturer must know its composition. The manufacturer should also define the limits of the detergent residue that are acceptable.
It’s also a requirement that the validation process does not support the growth of microbes. In determining if the validation process has supported microbial growth, the storage of the equipment before cleaning and after cleaning is often considered to decide whether they support microbial growth. Make sure that after cleaning the equipment is dry. Store it in a dry place. This is important as any other sterilization procedure that might be applied to the equipment will more likely achieve the required standard.
Samples are needed to determine the level of residues present in the equipment. There are two types of sampling used in the validation process. Rinse sampling and direct sampling. Direct sampling is used to collect samples for areas that are hard to clean. With rinse sampling, you can get a sample of a place that is inaccessible or for a large surface area. Using the two methods is highly recommended.
Calculating the Acceptance Criteria
A cleaning process is determined before the process begins. An appropriate method is determined by creating a matrix of the product’s attributes, and the equipment is used. The method chosen should be sensitive enough to detect any residuals on the equipment. The accepted method should also detect an acceptable limit of the contaminants and residues.
A proper cleaning method validation will enhance the process of the company’s equipment cleaning and will free the company from facing legal actions for not performing it. Therefore every company where a pharmaceuticals or whatsoever industries it operates in must always observe this process.