Industry Challenges ? Role of information management tools..!
One of the most important risks that faces drug companies today is that compliance to staggeringly stringent process standards of various aspects such as Good Manufacturing Practice (GMP), Good Clinical Practices (GCP) and Good Laboratory Practice (GLP).
The all operations of industry are under the vigilance of drug regulatory authorities that enforce high standards, enhances efforts, build trust of its end users and the obligation on the regulatory bodies to insure a great supply of quality drugs at affordable costs.
Countries like in India, where drug companies not only producing and also exporting drugs to the other countries thus drug companies need to adhere standards not only enforced by the national regulatory bodies also adhere with regulatory standards that are set by the international regulatory authorities to which the drug products are being exported. The regime of submission is becoming stronger as regulatory authorities expect for greater compliance from the companies imparted the mounting consumer pressures and enhancing health care standards.
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