Ensure the quality and integrity of pharmaceutical products with validation services

In a general term validate means giving a legal sanction to approve or confirm. Similarly, validation can be applied on a wide range of products, services or circumstances in order to ensure their quality. In the cold chain distribution industry- where it is compulsory to maintain a stabkle condition during the transportation of temperature sensitive and frozen products- validation is important to ensure the quality of the products during the shipping of the temperature sensitive products.

Vaccines and biological are temperature sensitive materials which require controlled temperature not only in the factory, but throughout the shipping of cargo.  If they are not manufactured or shipped under strict controls, they can not only lose their integrity, but also become hazardous to the consumers.  Several quality assurance organizations have formed in order to ensure the integrity and quality of these temperature sensitive products.  Some of these organizations which work in this field include FDA, WHO, GMP, GDP, HACCP, SFDA and MHRA compliance. These organizations have their guidelines which every pharmaceutical company or supplier should implement to ensure the quality and integrity of the products.

The validation procedure started for the quality control of vaccines and pharmaceutical during the manufacturing process. Nowadays, it is also applied to the cold chain delivery system to maintain the quality and integrity of the products during the manufacturing, packaging, storage, shipping and delivery of the pharmaceutical products.  

Many pharmaceutical companies prefer to hire third party service provider for getting excellent and reliable technical and validation services in the area of temperature and humidity sensitive distribution and storage. Hiring a third party company for quality compliance saves the time and effort of the pharmaceutical companies. There are different guidelines of different quality control organizations related to manufacturing, packaging, storage, shipping and delivery of the pharmaceutical products. Not all manufacturing companies have ideas about all these rules and regulations. Hiring a third party service provider for quality compliance provide peace of mind that everything is handled as per the industry standard and in a right way.

The professional service providers utilize the latest techniques and tools to ensure the quality and integrity of the pharmaceutical and other temperature sensitive products. Data logger is one of the devices which are widely for temperature and humidity monitoring after regular interval. Data logger comprises internal or external sensor which record the temperature and humidity after regular interval. The professional service providers are responsible for ensuring the quality and integrity of the temperature sensitive products right from packaging to delivery.

To get excellent and reliable validation services, 

visit www.compliance.com.sa.