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Customized Services


By analyzing drug development and the corporate goals for each of our clients, Pacific BioDevelopment develops and executes customized solutions to meet their unique objectives. We provide our clients access to a multi-disciplinary virtual team, across all phases of drug development as needed. Our goal is to develop long-term relationships with each client by providing drug development strategies designed to save time and money and drastically increase your chances of success.

Business Development

Assistance for license opportunities, business plan development, fund raising assistance, strategic alliances.

Manufacturing Technology

Strategic and technical assessments for API and Drug Product made under cGMP for drug and biological products.

Medical Affairs

Clinical development strategies, CRO selection/Audits/Transfer of Obligations, implementation of clinical trials, and more.

Nonclinical

Expertise in pharmacology and pharmacokinetics, toxicology, immunology, and more.

Quality Assurance

Good Manufacturing Practice (cGMP) and Good Clinical Practice (cGCP)/Good Laboratory Practice (GLP) services.

Quality Control

Audits of raw material vendors and testing facilities, evaluation of test methods and methods validation, and more.

Regulatory Affairs

Electronic submissions, labeling and promotional materials, regulatory affairs guidance and expertise.