Pick from a variety of dosage forms

Increase efficacy, bioavailability, adherence, and safety.

From Preformulation to Clinical

Formulations in every stage of development

About Renejix

With broad, deep-scale expertise in small molecule dosage development sciences, delivery technologies, and multi-modality manufacturing, Renejix Pharma Solutions is a Contract Development and Manufacturing Organization (CDMO) partner for your orphan drugs, blockbuster drugs, and generics, Renejix is a premium quality and price leader enabling pharmaceutical partners to slash time and costs across all dosage forms for small molecule product development, launch, and full life-cycle supply for patients around the world. 

Our scientists have unrivaled expertise in formulation development for complex dosage forms. We use a range of techniques to increase bioavailability or achieve controlled release for even the most challenging APIs. We have experience developing new formulation approaches and optimizing existing products, including oral solid dose (OSD), creams, emulsions, liquids, solutions, films, suspensions, and injectables.

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Benefits of working with Renejix

Why Renejix is Your Trusted CDMO Partner

Faster Time-to-Market

Cut up to 20 weeks of your early phase and late phase timelines!


Over 300+ state of the art equipment, 350+ employees, 2+ fully equipped facilities, and 20+ depots that can seamlessly adapt to your evolving needs from early development stages to large-scale production.

Quality Assurance

Ensure compliance with stringent industry standards, reducing your risk guaranteeing product integrity, and timely market entry with products that meet or exceed the highest quality benchmarks.

Expertise and Experience

Our seasoned managment team brings 30+ years of industry knowledge on average, ensuring your programs are guided by proven professionals.

Risk Mitigation

Address potential challenges from development to manufacturing from the get-go, ensuring consistent quality and regulatory compliance.

Our Capabilities

Your Challenges Handled from Preclinical to Commercial. 

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Technology Transfers
Scientists, engineers, & quality personnel dedicated to pharma tech transfers.

Pharmaceutical experiments

Preclinical Development

Screen your drug candidate is viable for further development and  ensure the safety of clinical trial participants.

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Pre-formulation, dosage design, process development, and scale-up with analytical methods for pharmaceuticals.

Methods Development and validation
Regulatory Services
Ensure global compliance, streamline approvals, & support product lifecycle with strategic regulatory planning & quality assurance.
Pharmaceutical Analytical Service

Analytical Services
Over 120+ analytical scientists to provide comprehensive analytical testing and method development for quality, validation, and compliance.

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Clinical Manufacturing
Our comprehensive services encompass Small, Pilot, Full-scale, and adaptive Manufacturing solutions across all phases of clinical trials
Supply management
Supply Management
Raw Material Sourcing, Vendor Management, Inventory Management, Demand Forecasting, Cost Optimization.
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Global Distribution
supply chain coordination, adherence to international shipping regulations, logistics, and ensuring product integrity across diverse markets and climate.
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Packaging & Labeling
Crafting compliant, stable global packaging with emphasis on material selection, tech & multilingual labeling for diverse patient needs.
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Commercial Production
Large pharmaceutical production that ensures quality, efficiency, compliance, advanced manufacturing, & streamlined processes for timely delivery.
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Portfolio Managment
Strategic planning & ongoing optimization for market impact, addressing trends, regulations, & tech advancements ensuring sustained relevance & profitability.