Aptuit, Inc.

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Description

Meeting the regulatory and clinical trial requirements, while ensuring your drug substance is developed into a successful drug product, can be one of the most difficult, involved and complex challenges of your drug development process. Our pharmaceutics department can deliver pharmaceutical development services to enable you to develop your drug substance into a drug product suitable for global markets, seamlessly and efficiently.

Although it is widely recognized that the development of inhaled products is fraught with challenges, Aptuit offers unique advantages to overcome them. Along with its experienced, integrated multidisciplinary team as cited, it is significant that the respiratory team works from one location, engaging in transparent, straightforward discussion throughout the process. Using the concept of Integrated Knowledge , they share in a careful, ongoing review of supporting data, striving to deliver critical project milestones and dedicated to exceeding client expectations.

Quality We strive to deliver the highest possible quality in the scientific services we provide to our customers. Only by doing so can we be considered leaders in our industry.

Although the industry has seen an increase in overall R&D spending the number of novel compounds making it to market has decreased. Drug innovators are faced with wading through thousands of compounds in order to get one to market, spending an average of 10 years in drug development . By speeding a potential compound into man, drug developers can make critical portfolio decisions, potentially saving millions of dollars and years in development.

Qualified Persons In line with EU cGMP requirements, we have designated Qualified Persons (QPs) who are available to provide either a full or partial certification step for Investigational Medicinal Products for use within the European Union. These Qualified Persons are available across several UK sites providing expertise and experience on a wide range of pharmaceutical drug development products to provide services in line with the EU Clinical Trials Directive.

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