Pharmaceutical raw materials identity testing is an important part of your drug development and manufacturing process. By testing raw materials to verify they are suitable for their intended use, you prevent production delays and problems.
BA Sciences, a qualified cGMP compliant raw material testing lab, performs USP, EP, BP, JP and NF testing, offering a complete pharmaceutical compendial testing verification solution.
Our experienced analysts can perform testing for all phases of CMC drug development through release testing. Whether you need raw material analysis or finished product testing, BA Sciences has developed protocols with your expectations in mind. We offer wet chemistry, instrumental analysis, release testing and stability testing. We are FDA registered, DEA licensed, cGMP compliant, and ISO/IEC 17025:2005 accredited.
There are many reasons why pharmaceutical raw material testing is a necessary component of the product development process. The most important is that FDA requirements include raw material identity testing as well as verification of their purity and quality. Another is that USP raw material testing and other methods help determine the attributes of ingredients, which can determine whether the end product will have unintended side effects. An additional important purpose these processes have is to inform manufacturers as to whether or not their sources and vendors are qualified.
