Best CRO Company in India

A CRO is an organization that provides support to the pharmaceutical, biotechnology and medical device industries in the form of research outsourced on a contract basis. It is a cost-effective solution to develop drugs or pursue new medicines. Specifically pertaining to CROs providing clinical-trials services, it means that a sponsor (e.g. a pharma company) can contract any organization to perform one or more of the sponsor’s trial-related duties and functions. The Clinical Research Company is continuously undergoing appositive development in India. Gradually the clinical researches are being viewed as drug discovery than drug development destination only, at present many companies are looking for innovations.



There are many CROs operating in India which can be divided into two major categories as Global Players with presence in India and Domestic players. Most of the domestic players are owned or supported by Pharma companies and very few are independent. Out of which Veeda Clinical Research established in 2004 at Ahmedabad in Gujarat, India is an independent Clinical Research Organization (CRO).

Veeda CR is a full-service CRO that conducts clinical research to support clients in their clinical programs. The company provides expert services in PK (pharmacokinetic) and PD (pharmacodynamics) studies in healthy volunteers; conducts patient trials in generic molecules and NCEs (new chemical entity) and undertakes research in Biopharmaceuticals. The company offers a fully integrated package that includes services on Phase I to Phase IV clinical trials in the central nervous system, oncology, and other complex therapeutic areas. The company's services also include clinical trial management services comprising patient recruitment and retention, project management, clinical monitoring, drug safety/pharmacovigilance, medical affairs, quality assurance, and regulatory and medical writing to meet global clinical development needs. Currently, Veeda is working with 10 out of the top 15 pharmaceutical companies across the globe. Veeda has an exemplary regulatory track record of completing 28 USFDA, 5 ANVISA, 4 WHO, 3 MHRA, 1 AGE, 1 ANSM, 1 MCC, 12 DCGI audits successfully to date.

With more than a decade of experience Veeda has now become one of the most desired partners to the pharmaceutical fraternity globally for conducting their clinical studies in India to deliver safe and quality solutions with no compromise on ethical practices. 

Veeda’s Expert Services:-

• BA/BE Studies

• Central Bioanalytical Services

• First-in-Man Studies

• Drug Interaction Studies

• Glucose Clamp Studies

• Patient PK Studies

• Clinical Trials

• Inhalation Studies

• PD Endpoint studies

• Complex Bioanalysis (Vitamins etc.)

• Elemental Bioanalysis

• Biosimilars/Immunogenicity Studies

• Pharmacovigilance Services