For well over 10 years, Excite Pharma Services has provided GMP Analytical Services that include R&D work, Method transfers, Method development, and a number of other analytical services. We knew back in 2009 when we started that we could put out a good sound product to an industry that was in dire need of quality and reliability. One of the things that has always set Excite apart is our practice of working WITH our clients, not for FOR them. We essentially become an extension of their team. Their project becomes our projects and we get down in the trenches with them to determine the best methods, the proper equipment and detector, and the optimal techniques to use in order to perform their analytical tests and ultimately get them the highest level of success.
There are many ways to conduct testing and some of it requires a special interface upon the introduction of the sample to the instrument. Or perhaps it might require a unique way of prepping or extracting out the product. Excite works with the client to establish to do these things while following all of the regulatory guidelines that maybe some of the other companies would baulk at and say they just don’t have the capability – or they’re not willing to. As long as we have the proper procedures in place to meet the clients’ needs, we will work with them to get it done. There are a lot of factors that go into onboarding a new client, but ultimately, there is no project too small or too complicated when it comes to the chemical projects Excite is willing to take on for our customers.
We hold ourselves to a higher standard on timelines, but we allow ourselves to remain flexible enough to accomplish what you require. Depending on what your project needs, we can work with you to get it done – even up to and including a facility change (as evidenced by our recent equipment and facility upgrades/ improvements, per client requests). We’re doing all of these things to meet the needs of our clients, so believe us when we say… we will go the extra mile to accommodate your project. That is something you won’t hear from most of our competitors.
At Excite Pharma, we also utilize program managers assigned to chemistry and manufacturing projects who make sure the testing is right for the client and confirming/verifying that all the work requested by the client is included in their contract and that the reports they need are generated on time and within the specs they needed. Our clients love our program management and we are actively seeking to grow our team of program managers.
We service the analytical department with HPLCs, UPLCs, GCs, ICPMS or Metals Analysis, and all of the identification testing and moisture content testing. We also do testing for the USP monograph, following all of those requirements. Excite Pharma recently passed an FDA and a general inspection without any written 483’s. The quality of work we do meets and exceeds the standards in a heavily regulated environment. We have a super strong QA department. When you look at anything with QA or chemistry or manufacturing, you want to make sure you’re not in a situation where your product – whether it’s the data or the actual manufacturing product – is compromised by any means, and having solid audits and a solid history free of written warnings, etc – that just shows that a provider has good procedures and that they are doing what is needed to meet or exceed expectations… like Excite Pharma.
So regardless of the size of your project, we would love the chance to talk with you about your manufacturing need and see if Excite can help you experience the growth our other customers have seen with their products.
