Data integrity and manufacturing compliance issues have stung Indian drug firms over the recent past, eroding both growth and reputation. And with the US Food and Drug Administration expected to increase its foreign pre-approval ANDA and GMP inspections in FY2019, the Indian pharma industry will likely need to cover significant ground to meet evolving compliance requirements and achieve sustainable excellence in quality and compliance.
Lachman Consultant Services, Inc, which is a leading provider of expert compliance, regulatory affairs and technical services to the life...
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