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Accelevate™ Early Development Service

AccelevateTM transforms the complexities of small-molecule early drug development into a streamlined, efficient process. From initial concept to clinical readiness, our platform simplifies every step, delivering IND-enabling data and clinical trial materials in under 100 days—because time matters.
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From Idea to IND-Ready in 100 days

Benefits
Capabilities
Why choose AccelevateTM?
Get fast, phase-appropriate early drug development services perfect for:
  • Virtual labs and small pharma who need to determine viability fast.
  • Small molecule formulations for parenteral drug delivery.
  • Aqueous or oily solutions that can be filter sterilized.
  • Immediate release profiles.

Your Molecule’s Journey to Clinic

Your drug’s early drug development is unique, but our roadmap ensures nothing is left to chance.

Robust formulation development solves for composition and stability.

Release to Clinic with IND filing-ready from smooth submissions.

30+
years of experience in small molecule formulations
400+
development programs completed
60+
NDA Filings Supported

Expertise Where It Counts

With over 30 years of small-molecule formulation experience, Pii is the trusted partner for complex early drug development. Our team of scientists has completed 400+ early development programs. But we don’t stop there—if your early clinical trials succeed, we seamlessly scale production to support late-phase trials and commercial supply.
From discovery to delivery, our expertise ensures that your project is in the best hands.

Behind the Scenes: Where Speed Meets Precision

Take a closer look at how our early drug development services and small-scale clinical manufacturing prioritize you and your drug product. From groundbreaking R&D to expert small-scale fill-finish services, our videos showcase the precision and care that drive every project forward.
R&D & Analytic for Early-Stage Development
Robotic Small Scale Aseptic Fill-finish production

Quality Built for Every Phase

At Pii, we deliver reliable, regulatory-compliant data tailored to each stage of development. Our phase-appropriate early drug development services focus on speed and flexibility, while later phases emphasize rigorous validation to meet commercial standards.
From development to scale-up, our expert team adheres to cGMP guidelines, ensuring every batch meets the highest quality standards. With Pii, you get data you can trust—delivered on time, every time.

Ready to AccelevateTM your molecule?

Let’s turn your vision into reality - fast!

Looking Ahead: AccelevateTM for Oral Dose Drugs

Our commitment to innovation doesn’t stop here. AccelevateTM is expanding to include oral dosage forms, bringing the same speed and precision to even more development pathways. Stay tuned for more details!
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