Contract Research

Oasis Research Center

A symbol of quality contract research for pharma sector

Oasis Contract Research Center (CRC) offers a wide range of services to global research based pharmaceutical companies. The services provided are in the domains of drug formulation, trouble shooting, software, validation etc.

We trust in integrity, confidentiality and quality of the research solution and we can be a valued partner to your research team and drug discovery process.

The strength of the center in R&D is complemented through closed and formalized collaborative work with eminent scientists from reputed universities and institutions.

The facilities at the center are manned by scientists holding M.Pharm / Ph.D. with vast experience in F&D, from lab scale to commercial scale. The center has a multidisciplinary team based approach to the challenges posed by the pharma industry.

The center has excellent facilities and contracts with prestigious academic institutions to undertake high tech research, for experimenting innovative ideas.

Pharma research is an integral part of R&D comprising of formulations, packing and analytical development department. We deliver various types of new dosage forms for manufacturing locations complying with their regulatory requirements. The dosage forms include solids / liquids / parenterals / pellets / cosmetics.

 

Research facility

Oasis contract research center, Oasis CRC, has pooled resources of all its organizations and affiliates. Its exclusive labs for drug development and industrial pharmacy located at Jaipur, have many researchers. Philosophy of Oasis CRC is aimed at providing cost effective and fast track solutions in the following:

  • Pharmaceuticals, Cosmeceuticals, Nutraceuticals
  • Product development, Production trouble shooting
  • Quality audit, Regulatory affairs
  • Analytical development, Synthetic chemistry

 

Solutions offered

  • Designing of production and testing facilities
  • Product development
  • Analytical method development
  • Analytical method validation
  • Stability studies as per ICH guidelines
  • Microbial studies
  • Process optimization and SOP writing