Computational Infrastructure for Modern Pharmaceuticals

June 19, 2019

This paper, authored by Alireza Shabani, Founder & CEO of Qulab, describes the necessary computational architecture for pharmaceutical firms to accelerate R&D and drug discovery, especially utilizing special purpose silicon and quantum processors.

Spotlight

Butterworth Laboratories

Excellence in Analytical Chemistry Since 1974 With 40 years experience, Butterworth Laboratories remains a fully independent UK contract analytical service providing Quality Control Testing, Method Development & Validation and Stability Study Storage & Testing to the pharmaceutical and related industries. We work in partnership with our clients who not only recognise our expertise in analytical chemistry and standards of service but also value our integrity and impartiality. Our regular inspections by the MHRA, UKAS and FDA ensure that the service you receive is at the very highest level for testing, validation and analysis.

OTHER WHITEPAPERS
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A BLOCKCHAIN TO ENSURE COUNTERFEIT FREE PHARMACEUTICAL SUPPLY CHAIN

whitePaper | February 5, 2022

Essential medicine access is one of the main objectives of healthcare systems in and pharmaceutical supply chains ensure that the right amount of medicine, with acceptable quality, will reach the customers in need

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Access to medicinal products

whitePaper | January 3, 2022

There are many factors that can prevent a patient from being able to obtain the medicine they need, ranging from selective marketing decisions by companies to products being too expensive or pharmacy stock-outs

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A Vision for the Global Generic and Biosimilar Medicines Industry

whitePaper | May 22, 2021

One of the key roles of the generic and biosimilar medicines industry is specifically to promote the widest possible access to affordable medicines with high quality, safety, and efficacy for patients globally by introducing competition into the markets. Despite the many hurdles, the generic medicines companies have clearly lived up to the challenges posed by the pandemic as it is an industry that is quick to adapt and agile in manufacturing scale-up. During the outbreak of COVID-19, this industry was providing most of the medicines needed in Intensive Care Units to ventilate critically ill COVID patients. It is also providing most of the quality medicines dispensed around the world, especially for increasingly prevalent chronic diseases and is therefore a strong contributor to health outcomes globally.

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Research and Development in the Pharmaceutical Industry

whitePaper | April 1, 2021

Every year, the U.S. pharmaceutical industry develops a variety of new drugs that provide valuable medical benefits. Many of those drugs are expensive and contribute to rising health care costs for the private sector and the federal government. Policymakers have considered policies that would lower drug prices and reduce federal drug expenditures. Such policies would probably reduce the industry’s incentive to develop new drugs.

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Application Notes & Whitepapers 2019

whitePaper | December 19, 2019

Welcome to European Pharmaceutical Review’s Application Notes & Whitepapers Supplement 2019. This year’s topics range from analytical techniques for bioprocess investigation, host cell protein analysis and Raman imaging to advice on outsourcing services for product characterisation.

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Paving the way for pharma R&D to use FAIR data

whitePaper | December 16, 2019

The use of FAIR (Findable, Accessible, Interoperable and Reusable) data in drug discovery and development could be transformational. But the pharma industry has been slow to embrace FAIR data — partially because of difficulties in establishing the necessary infrastructure and because of internal culture.

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Spotlight

Butterworth Laboratories

Excellence in Analytical Chemistry Since 1974 With 40 years experience, Butterworth Laboratories remains a fully independent UK contract analytical service providing Quality Control Testing, Method Development & Validation and Stability Study Storage & Testing to the pharmaceutical and related industries. We work in partnership with our clients who not only recognise our expertise in analytical chemistry and standards of service but also value our integrity and impartiality. Our regular inspections by the MHRA, UKAS and FDA ensure that the service you receive is at the very highest level for testing, validation and analysis.

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