Services

CRO

CRO

At YNR Laboratories, we are your trusted partner in pharmaceutical research and development, offering a full spectrum of Contract Research Organization (CRO) services to pharmaceutical, biotechnology, and specialty chemical companies worldwide. Our extensive expertise, combined with advanced technologies and a steadfast commitment to excellence, allows us to streamline and accelerate the drug development process. By partnering with us, you gain access to our state-of-the-art facilities and a team of skilled professionals dedicated to advancing your projects efficiently and effectively. We are committed to bringing life-changing therapies to patients faster, ensuring that groundbreaking treatments reach the market with the highest standards of quality and innovation.

Investment Plan


Key Capabilities -Custom Synthesis
  • Reference Compound Synthesis
  • Synthesis of scaffolds, building blocks for Medicinal Chemistry and Parallel Synthesis
Diverse Organic Synthesis -Custom Synthesis
  • Aliphatic, alicyclic, aromatic
  • Heteroaromatic
  • Macrocycles - Speciality in building blocks for library synthesis
  • Peptide Synthesis - Solid and Solution Phase, IRORI technology

Why Choose Us?

With years of experience in the pharmaceutical industry, we have successfully managed numerous clinical trials across diverse therapeutic areas.

We offer flexible and customizable solutions to meet your unique project requirements and timelines.

Our dedicated team is committed to delivering superior results with a focus on accuracy, efficiency, and integrity.

Clinical Trials Management

We offer end-to-end solutions for Phase I-IV clinical trials, including protocol development, site selection, patient recruitment, monitoring, and regulatory submissions..

Clinical Trials Management

We offer end-to-end solutions for Phase I-IV clinical trials, including protocol development, site selection, patient recruitment, monitoring, and regulatory submissions..

Biostatistics and Statistical Programming

We provide expert statistical analysis and programming services to support clinical trial design, sample size calculations, and data interpretation.

Regulatory Affairs

Our regulatory experts navigate complex regulatory landscapes, ensuring compliance with global regulations and expedited approval processes.

Medical Writing

From study protocols and clinical study reports to regulatory submissions and publications, our medical writers produce high-quality documents tailored to your specific needs.

Quality Assurance and Compliance

We maintain the highest standards of quality and compliance throughout the drug development lifecycle, safeguarding data integrity and patient safety.

services