Pharmaceutical Manufacturing Leveraging.cdr
نویسنده
چکیده
Ashok Khanna has over 19 years of industry experience in the field of healthcare, hi-tech and telecom. As a business leader, his expertise spans multiple medical and pharmaceutical domain areas including new product development, product lifecycle management, manufacturing operations management, R&D and quality, regulatory and product sustenance. With over 21 years of experience in the IT industry in areas such as software development, research, technology consulting and software quality assurance, Prateep Mishra leads the development of platforms for Internet-of-Things applications. Mishra's current focus areas include IT infrastructure architecture and design, IT transformation, storage systems, large scale and real time analytics platforms, and cloud computing. Mahendra Hasnabis has 17 years of engineering and manufacturing IT experience covering various functions such as consulting, solution architecture, design development, project and program management. Hasnabis has been contributing extensively towards enterprise-wide initiatives including standardization, rationalization and manufacturing transformation. Pharmaceutical manufacturing plants across the world will soon encounter radical changes in their operations, with the increasing use of sensors on the manufacturing floor. This network of sensors which can drastically improve patient outcomes is referred to as the Internet of Things for Pharmaceutical Manufacturing (IoT-PM). Connected manufacturing technologies have gained prominence as a result of the growing incidence of counterfeit drugs and the need to monitor drug quality and distribution. A connected manufacturing environment offers seamless and integrated access to information from shop floor to top floor, as well as through the distribution channels. Regulatory agencies and manufacturers can track the flow of pharmaceuticals through channels where serialization of information is used or updated. Improved visibility and remote access to equipment improves overall performance of the plant and reduces the cost of production through timely supervision. IoT-PM simulates an environment where equipment parameters will get transmitted by shop floors via a gateway onto the internet to be stored, aggregated and analyzed. This application will be capable of storing data for multiple pharmaceutical manufacturing plants. It will analyze data and report exceptions in real time to promote global visibility and control of manufacturing operations, and optimize performance.
منابع مشابه
Piracetam 800mg Tablets, Piracetam 800mg Tablets India, Piracetam 800mg Tablets manufacturers India,
Tablets brand, contains, Piracetam 800mg Tablets India, Piracetam 800mg Tablets side effects, Piracetam 800mg Tablets use, Piracetam 800mg Tablets overdose, Piracetam 800mg Tablets drug, Piracetam 800mg Tablets composition, Piracetam 800mg Tablets Manufacturing, Pharmaceutical manufacturers, Piracetam 800mg Tablets contains, Piracetam 800mg Tablets Manufacturing, Piracetam 800mg Tablets Pharmac...
متن کاملBENZYL PENICILLIN, BENZYL PENICILLIN India, BENZYL PENICILLIN manufacturers India
PENICILLIN India, BENZYL PENICILLIN side effects, BENZYL PENICILLIN use, BENZYL PENICILLIN overdose, BENZYL PENICILLIN drug, BENZYL PENICILLIN composition, BENZYL PENICILLIN Manufacturing, Pharmaceutical manufacturers, BENZYL PENICILLIN contains, BENZYL PENICILLIN Manufacturing, BENZYL PENICILLIN Pharmaceutical manufacturers, BENZYL PENICILLIN side effects, BENZYL PENICILLIN use BENZYL PENICILL...
متن کاملSketching Out the Hidden Lean Management Principles in the Pharmaceutical Manufacturing
In Recent times, pharmaceutical companies are faced with the demanding tasks such as adjustments to the unstable and turbulent market in times of economic crisis as well as to meet the customer needs. The pharmaceutical industry, manufacturing in a current Good manufacturing practice (cGMP) environment has been slow to adopt the lean manufacturing unlike many sectors where it has been successfu...
متن کاملWHO Expert Committee on Specifications for Pharmaceutical Preparations.
The Expert Committee on Specifications for Pharmaceutical Preparations works towards clear, independent and practical standards and guidelines for the quality assurance of medicines. Standards are developed by the Committee through worldwide consultation and an international consensus-building process. The following new guidelines were adopted and recommended for use: procedure for adoption of ...
متن کاملRECENT RESEARCH ON QbD APPROACH IN FORMULATION DEVELOPMENT - A REVIEW
QbD is a systemic approach to pharmaceutical development. It means designing and developing formulations and manufacturing processes to ensure predefined product quality. Some of the QbD elements include defining a target product quality profile, designing product and manufacturing processes, identifying critical quality attributes, process parameters, and sources of variability and controlling...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2014