Our Services

Green Ridge Consulting guides clients through the drug development process, from initial strategic planning to detailed technical execution, utilizing a science-based approach and a fundamental understanding of drug delivery technology.

Our services include:

Dosage Form Development

From initial selection of the right dosage form for your drug substance and program needs, through formulation, clinical manufacture, and scale-up, GRC provides work plans, analyzes data and rigorously oversees a program throughout the drug development process to ensure a robust pharmaceutical product in a cost and time-efficient manner.

CRO/CMO Selection & Management

GRC carefully and thoughtfully identifies and manages contract outsources to meet each client’s specific and individual project needs for drug product formulation and development.

Due Diligence

GRC’s due diligence services support product acquisition with in-depth analysis to guide the purchase or licensing of viable pharmaceutical formulations. The GRC team critically evaluates the likelihood of technical success and potential competitive approaches on behalf of prospective pharmaceutical investors.

Intellectual Property

GRC provides exceptional Intellectual Property (IP) support including the creation of IP and a keen understanding of existing IP landscapes in specific drug delivery areas. Our group has also utilized their technical knowledge in support of expert witness services for a range of clients. The Green Ridge team members are inventors on 45 patents and patent applications.

Regulatory & Technical Writing

GRC specializes in regulatory writing for the drug product Chemistry Manufacturing and Controls (CMC) sections for Investigational New Drug Applications (INDs) and New Drug Applications (NDAs), as well as technical reports to support filings.