Industrial Production Processes (IPP) has announced it is the official distribution partner of CS Analytical Laboratory - a cGMP, FDA-registered and inspected contract laboratory exclusively designed and dedicated to container testing for the pharmaceutical, biotechnology, and medical device industries - in the UK and Ireland.
Under the agreement, IPP will represent and promote the CS Analytical service offering to its key clients in need of routine USP and EP container qualification testing and USP 1207 integrity testing across both territories.
Routine container qualification testing has become much more stringent and intense due to recent changes to the standard USP methods. Clients globally are looking for service providers that understand the complexity of these unique requirements and have the laboratory experience to execute the qualification testing required. CS Analytical is wholly focussed on this market and can assist clients in defining the required qualification methods and help to ensure that they are done in a cGMP, FDA regulated laboratory. With the growth of the USP 1207 container integrity testing requirements, IPP clients who are purchasing instruments commonly need an experienced service provider to assist with method development and validation.
CS Analytical CEO Brian Mulhall said: “IPP has a long and established history in the package equipment field and their ability to promote the CS Analytical testing program will enable them to better serve their client based on multiple fronts.”
IPP’s managing director Jack Daly added: “Partnering with CS Analytical was an easy and natural decision as we are already well established in the packaging equipment field and its cGMP laboratory testing offering allows the IPP team to better serve our client base with a broader, necessary and unique service offering.”
