Celebrating nearly 30 years in Business

Pacific BioDevelopment, LLC was founded in 1996 with the mission of providing a range of high quality strategic and integrative services to the biotechnology and pharmaceutical industries.

Pacific BioDevelopment, LLC was founded in 1996 with the mission of providing a range of high quality strategic and integrative services to the biotechnology and pharmaceutical industries.

01.

The development of a prescription drug that gains marketing approval costs an average of

$ 0 billion

and is often a process that takes more than ten years.

*Source: Deloitte Measuring the return from pharmaceutical innovation – 14th edition 2023

Get to Know us

Customized Solutions for Drug Development

Pacific BioDevelopment consultants cover the full range of drug development to commercialization.

01.
Our goal is to develop long term relationships with each client by providing comprehensive drug development strategies designed to maximize capital efficiency and accelerate time to approval.
02.

We have over

0 years

of experience in the field since we openned in 1996.

03.

We have advised more than

0 +

companies worldwide in strategic drug-development.

Business Development Manufacturing Technology Medical Affairs Nonclinical Quality Assurance Quality Control Regulatory Affairs
Business Development Manufacturing Technology Medical Affairs Nonclinical Quality Assurance Quality Control Regulatory Affairs
Our Solutions

Customized Solutions for Drug Development

The development of a prescription drug that gains marketing approval costs an average of $2.3 billion* and is often a process that takes more than ten years.

*Source: Deloitte Measuring the return from pharmaceutical innovation – 14th edition 2023

Pacific BioDevelopment opened its doors for business in 1996. Since then, we have provided strategic drug-development advice to more than 500 companies worldwide.

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.

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.
Who We Are

Our Firm

Our mission at Pacific BioDevelopment is to provide the highest quality integrated drug development strategies in order to facilitate timely and cost efficient proof-of-concept results, entry into the clinic, or market approval.

About Us

Now

They trust in us

Our Clients

Pacific BioDevelopment consultants cover the full range of drug development to commercialization.

01

Start-Ups

Early-stage companies have extreme pressure to get drug candidates into the clinic quickly to show initial promise to enable partnering or to gain additional funding.

02

Mid-Sized Biotechnology and Pharmaceutical Companies

Mid-sized biotechnology and pharmaceutical companies provide much of the innovation that fuels the medical industry.

03

Multinational Biotechnology and Pharmaceutical Companies

Multinational biotechnology and pharmaceutical companies need expertise across global markets and in all aspects of development to ensure they maximize the market potential of their drugs.