Clinical Trials Compounding

Compounding for Clinical Trials

Partner With Maida Pharmacy

Maida Pharmacy provides precise, compliant, and flexible compounding services to support pharmaceutical and academic research.

Quality, Compliance, and Expertise

Where Science Meets Precision

We operate under strict USP compliance to ensure every formulation meets research and safety standards. Our internal QA/QC team continuously reviews, tests, and documents every process to maintain accuracy and consistency.

503A Compounding

503A Compounding

We operate under strict USP compliance to ensure every formulation meets research and safety standards.

QA/QC Program

QA/QC Program

Our internal QA/QC team continuously reviews, tests, and documents every process to maintain accuracy and consistency.

Regulatory Expertise

Regulatory Expertise

We work closely with regulatory frameworks and guidance to ensure your trial materials meet all applicable requirements.

Laboratory Liquid Compounding Process
Laboratory Powder Compounding Process

Flexible Solutions for Research Teams

Formulation Without Limitations

We support early exploratory trials by compounding microdoses, validating stability, and optimizing delivery parameters for Phase 0, 1, and 2 trials.

0

Phase Zero

We support early exploratory trials by compounding microdoses, validating stability, and optimizing delivery parameters.

I

Phase One

We compound small-scale formulations for human safety trials, enabling dose escalation studies with tight tolerances.

II

Phase Two

We produce intermediate-scale batches to test efficacy and refine dosing in patient cohorts under blinded conditions.

Dosage Form Versatility

  • Oral Medications Including Capsules, Suspensions, and Solutions
  • Modified Release Formulations
  • Topical Delivery Systems - Creams and Gels
  • Alternative Bases for Improved Drug Delivery
  • Nasal Sprays

Personalization

  • Small Batch
  • Blinding or Unblinding
  • Unique Strengths of Active Pharmaceutical Ingredients

Efficient, Compliant, and Cost-Effective

The Maida Advantage

503A Model of Compounding

  • USP Chapter compliance instead of cGMP
  • Lower project costs
  • Access to critical formulations

Quality Assurance & Control

  • Internal QA/QC team oversight
  • Regulatory collaboration

Logistics & Operations

  • 90+ years of compounding experience
  • Comprehensive product transport, storage, and distribution
Pharmaceutical Capsules

Let’s Discuss Your Next Study

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