As an industry-leading generic pharmaceutical manufacturer, our client was looking for support in the development, validation and implementation of updated stability indicating methods to maintain compliance with regulations.
A global leader and manufacturer of medical devices needed our support for the method development and validation of a 'clean in place' procedure which adequately detects traces of flush solvent.
Finding the right laboratory to provide you with analytical support is an important strategic decision. In our infographic, we highlight the key analytical services we deliver that will support your products through the drug development pathway.
Whether you're outsourcing to a contract laboratory or re-transferring methods in-house, this checklist of method transfer activities will help you cover all bases. In addition to these activities, make sure you consider the requirement for new equipment or resource and control these changes as appropriate.
Looking to take your ENDS products to new markets? Compare the differences and get the pros and cons between products with EU Tobacco Products Directive (TPD) notification and products with an EU medicinal product license in our free download.
Here at Broughton Laboratories we are a full analytical service provider with state-of-the-art facilities. View our full list of in-house techniques and capabilities here.
Selecting the right laboratory for quality control services is important to ensure you maintain customer satisfaction. We provide our clients with a dedicated team to deliver a tailored service that meets the changing demands of your supply chain.
Partnering with a contract laboratory is a long-term investment and must be decided upon carefully. Our white paper highlights the key areas to look for when selecting the right laboratory to partner with.
Are you looking to ensure your ENDS products remain compliant to regulations? Download our free PMTA Deadlines Leaflet to see what actions are required next.