Therapeutics

When you think outsource your drug development clinical project, you think of the one who can stand up for you and deliver. At ClinAsia it is ensured that you shall feel us as an extension of your own team.

Our task on hand is to drill down in to our expert resources and ensure driving your project successfully on time with a value addition. Superior solutions, proactive service and a personal approach are the trademarks of ClinAsia which makes it as the most preferred partner to many clients in Asia and globally.

It is most important and necessary that you work with a clinical research organization that has highly organized expertise in clinical development and has the most critical clinical and therapeutic expertise to meet your requirements and expectations. At ClinAsia we have a significant range of local and global therapeutic expertise, and in many therapeutic areas ClinAsia knowledge is second to none.

ClinAsia specializes in the following Therapeutic areas:

• Cardiovascular
• Oncology
• Central Nervous System
• Dermatology
• Immunology
• Hermatology
• Opthalmology
• Pediatrics
• Urology
• Respiratory
• General Medicine
  
  

PreClincal Services

PreClinical Services

ClinAsia daily schedule consists of developing programs to provide correct information about the chemical making of a new drug, its safety, its formulation strategy and its administration procedure to be followed when provided to the first man.

Using past data about the chemical making, we help our customers create an effective regulatory strategy formulation for good laboratory practice, toxicology and metabolism clinical studies required to support first-human studies.

Non-Clinical Development Program

Previously made development programs to avoid early chemical complexities in Clinical Trials.

Preclinical Estimation

Our experts at ClinAsia provide a complete range of research services to clients to select the most suitable study design and additional screening method for an investigational agent and there by maintaining the Preclinical estimation.

Chemistry, Manufacturing and Controls Consulting

Taking into account our customers manufacturing facilities, ClinAsia provides regulatory guidance to suit specifications, method creation and validation as well as co-coordinating stability studies.

Pharmacology and Toxicology

ClinAsia has extensive expertise in pharmacology with preclinical efficiency, efficacy, General Toxicology, Special Toxicology, Genetic Toxicology, reproductive and development toxicology, Safety pharmacology to guide clients through the preclinical phase.

Regulatory Submissions

ClinAsia has extensive experience preparing all major regulatory submissions, including complex multinational submissions for any type of drug applications.

www.clinasia.com