Pace Analytical Life Sciences Clinical Trial MaterialsWith Pace® Life Sciences, you have a partner who understands the unique requirements of your business and industry; one who can provide the technical expertise, innovation and world-class facilities that enable you to bring products to market faster and meet all the current quality, health and safety standards. For more than 30 years, Pace® has been advancing candidates from early pre-formulation and tox studies to an IND filing and on through the clinical phases. Our extensive GMP clinical supplies manufacturing capabilities include oral/solid/liquid and topicals capabilities, sterile fill-finish and clinical packaging and kitting for a variety of molecules/dosage forms.

Explore Our Services​

Pace® Life Sciences has decades of practical formulation development experience and expertise with sterile and non-sterile products, oral or topical dosages. Our attention to detail helps us create an appropriate formulation for your drug product that is safe, pure, and effective. Our formulation strategies will withstand FDA scrutiny and accelera

With more than 20 years of experience in pharmaceutical research and manufacturing, we understand the specific challenges aseptic fill-finish and manufacturing presents. Our facility is carefully designed with the flow of personnel and materials in mind, which follows current Good Manufacturing Practices (cGMP) guidelines and minimizes contamin

We follow current Good Manufacturing Practices (cGMP) in our clinical supplies manufacturing, packaging, and labeling services for domestic and international studies. Entrust your tablets, capsules, and powders to our experts so your clinical trials can proceed with ease.

We provide cGMP clinical supplies manufacturing, packaging, and labeling services for domestic and international distribution studies. Entrust your liquids, suspensions, and semi-solids to our experts so your clinical trials can continue with ease.

Pace® offers small scale feasibility and current Good Manufacturing Practices (cGMP) pilot scale processes for bioavailability enhancement of orally administered small molecules.

Our team of formulation experts design lyophilization cycles using both the develop of experiments (DoE) approach and SMART. This process is performed in an iterative manner in parallel with product formulation development.

We effectively deliver high-quality clinical supplies with our strong suite of analytical services. This reliable analytical data keeps your program on schedule throughout every step of process development, formulation development, and the manufacturing of clinical trial materials.