Opportunities and Challenges of Oncology Clinical Trials in India

Oncology Clinical trials are research studies that call for people. Through Oncology clinical trials, doctors find new methods to ameliorate treatments, quality and value of life for people with disease.

Researchers design oncology clinical trials to investigate new ways to:

• Treat cancer
• Find and diagnose cancer
• Prevent cancer
• Manage symptoms of cancer and side effects from its treatment

Oncology clinical trials are the full and final step in a long method that begins with research in a laboratory.

With well-developed medical education and a long-standing experience, a rock-hard information technology infrastructure, the presence of numerous institutions and laboratories with state-of-the-art equipment, India is a great platform for global market to conduct oncology clinical trials and to offer cheaper, safer, and effective treatment options to its afflicted population. Country like India having increased cancer load, have started considering clinical trials as a treatment alternative to the patient pools. With colloquy between the regulators, experts and stakeholders from industry, the regulatory environment has significantly improved in last few years.

Increasing cancer burden throughout the world and appreciable research spending in targeted cancer therapies, Oncology clinical trials undertaken in this therapeutic area has increased remarkably. Countries like India with its improved regulatory environment investigators and infrastructure offers opportunities to pharma companies to conduct their clinical trials in India in a cost-effective way. 

Why Are Oncology Clinical Trials Important?

Today, people are long lasting from effective cancer treatments that are the results of previous oncology clinical trials. Over the oncology clinical trials, doctors’ control whether innovative treatments are safe and effective and work better than current treatments. Oncology clinical trials also support us to innovative ways to prevent and detect cancer. And they help us progress the excellence of life for people during and after treatment.

When you take part in an oncology clinical trial, you add to our information about cancer and support recover cancer care for future patients. Oncology clinical trials are the key to making development against cancer.

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