Granulation Technology, Inc. is a chemical and pharmaceutical manufacturing and distribution company that has been in business since 1997 successfully serving small to Fortune 500 companies. GTI is a FDA GDUFA listed facility. It is a fully functional 35,000 sq. ft. cGMP facility. DEA Registered to handle Class III - V controlled subtances. We have been consistently adding to our large list of clientele ensuring their high demands for quality & safety standards in their products are met. At Granulation Technology, Inc we strive to provide the highest quality products that comply with FDA regulations, meet USP and are manufactured under GMP and ISO standards. This approach insures high quality products while providing cost competitive advantages.
We have capabilities to carry out the following analytical development activities in addition to method validations, which adhere to highest quality standards and regulatory compliance:
- Analytical Method Development & Method Validations
- Forced degradation studies
- Cleaning method
- Stability studies
- Dissolution and drug release profiling
- Raw material and packaging material testing
- Stability monitoring as per ICH guidelines
- Release testing and particle size analysis