Green Ridge Consulting

Founded in 2007, Green Ridge Consulting provides support to pharmaceutical and biotech companies in the field of drug product development. With over 80 years of combined experience in the field, our team provides technical guidance for the selection of API solid form and formulation strategy, process development activities and regulatory filing, as well as ensures oversight of work conducted at Contract Research and Contract Manufacturing Organizations recommended based on the development strategy.

We provide strategic and tactical guidance for development of new drug products including:

  • Solid form selection and solid state understanding in API and DP
  • Crystallization process development, optimization and troubleshooting
  • Optimization of API powder properties
  • Selection of dosage form and formulation approach
  • CRO/CDMO selection
  • Technical project management
  • On-site technical oversight
  • Review of batch records
  • Technical writing in support of regulatory submissions
  • Technical review of solid form, formulation, and process patents
  • Litigation support

GRC has a proven track record of delivering creative, science-based design, drug product development solutions for clients worldwide, including four of the top ten pharmaceutical/biotech companies in the United States and overseas, as well as more than 100 small and mid-size pharmaceutical/biotech companies.