The Important Role of Technology Transfer in Pharmaceutical Industry-a Review

Abstract

The Technology Transfer is both integral and critical to drug discovery and development process for new medicinal products this process gives necessary information for technology transfer from R&D to PDL department and development of existing product to the production for commercialization. The finishing product during manufacturing as well as assure constant quality transferred the situation for developing countries is controversial because it denied people with technical skills from developed countries to developing countries do not migrate the process of movement of technology from one unit to another. The transfer may be said to be successful if the receiving unit and the transferee can effectively utilize the technology for business gain.Technology transfer plays a vital role in the process of drug discovery to the product development and the full scale commercialization the article attempts to discus about the pharmaceutical technology transfer process steps, reasons and importance of technology transfer and the issues involved in the technology transfer in the pharmaceutical industry. Given technology centrality to development and technology acquisition necessity by developing countries for further development and benefit it is desirable to generate transfer and diffuse the best available pharmaceutical technology in these countries through product development and scale-up technique a commercialised drug product and to highlight how technology is transferred, importance of technology transfer, rezones for technology transfer, factors influencing technology transfer, drivers and barriers. The ultimate goal for successful technology transfer is to have documented evidence that the manufacturing processes for drug substances and drug product.

An Overview of Technology Transfer as a Regulatory Aspect

“…• Various parameters and processes are controlled to justify the accepted parameters throughout the development [8,9]. preliminary research ending with clinical research to the manufacturing of new drug products.…”

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“…According to WHO outlined as a logical procedure that controls the transfer of any method alongside its documentation and professional expertise between development and manufacture or b/w manufacturer site 4 . It is useful to build up dosage form in various ways because it provides efficiency in development, maintains quality of product, helps to realize a standardized process that facilitates price-effective production 5 . There are 3 standards in the definition of technology:…”