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The manufacturing industry is often regarded as one that is at the forefront of technology adoption. However, on the other side of the coin, there are many manufacturers, particularly in the medical device and biotech manufacturing domain who continue to rely on a paper-driven process. This makes it very easy for manufacturers to cut corners--manufacturing sub-par quality goods for customers. “This practice does not force the manufacturers to collect the right data, and in case the data collected is out of specification, it will not prevent the manufacturing process from continuing. Especially, in the case of the medical device industry, where it is critically important to prevent errors and prevent defects from eventually getting to the patient,” says John Dzelme, Global COO of Seabrook Technology Group— a Manufacturing Execution Systems (MES) solution provider that is catering to the Medical device and biotech industries. 

