The pharmaceutical industry has a zero tolerance to defects. This requires that all components that attribute to a manufacture of a quality drug should also follow the strict regulatory compliance. This is true for any application software that contributes to the manufacture of the drugs. With over 13 years of experience in providing solutions and more than 40 installations in the pharmaceutical industry, Base understands the nuances and the criticality associated with the industry. This accelerates the implementation of the solution. Our clients do not have to educate our consultants on the Pharmaceutical process. Our clients and consultants focus on leveraging the proven capabilities of E12 Pharma for their organization. Base E12 has been validated under the strict norms of 21CFRpart 11 of USFDA in a number of our client installations within India and the Americas.