How is New Drug Launched?

Before its launch in the market, each new drug research must undergo regulatory and ethical approval before executing actual research and launching the drug. Clinical research by the clinical trial study team must be conducted as per ICH GCP, maintaining compliance and following stringent regulatory guidelines.

Once the clinical research team’s research work is completed, the report is reviewed by USFDA, and they may perform site inspections. After completing all such steps, a new drug is launched in the market, delivering life-changing medicines to people needing them the most.

Each new drug research must undergo regulatory approval and ethical approval before execution of actual research. Clinical Research must be conducted as per ICH GCP and following stringent regulatory guidelines. Ongoing research work is also continuously monitored by various stake holders. Once research work is completed, report is reviewed by USFDA and may perform site inspections. After successful completion of all such steps, a new drug can be launched in market.

Encouraging New Clinical Studies

Appropriate conduct, adequate reporting, and accurate documentation are paramount in clinical trials. Though complex, they are extremely rewarding for investigators or researchers that have a passion for science and want to improve patient care.

At Central Health Solutions (CHS), we are committed to supporting and encouraging new clinical trials. As clinical research providers, we encourage organizations and stakeholders to start new clinical studies by providing them with a competent clinical trial team.

We provide our services for the ease of execution, the safety of participants and the clinical trial team, appropriate conduct, and documentation. CHS’s clinical study team will be happy to encourage and collaborate with new investigators who want to conduct clinical studies. We can help sponsors by providing appropriate study and research sites for the research activities.

Appropriate conduct, adequate reporting and accurate documentation is of paramount importance

Central Health Solutions (CHS) is committed provide its services for the ease of execution, safety of participants, appropriate conduct and its documentation.

CHS will be happy to encourage and collaborate with new investigators who wants to conduct the clinical studies.

We can help sponsors by providing appropriate study sites for the research activities.

CHS Has Team Exposed To:

• Oncology
• Psychiatry
• Dermatology
• Infectious
• Disease
• Cardiovascular
• Diabetes
• Chronic Kidney disorder
• Pain indications in research

Making Communication Easier for Investigators and Researchers

No matter the type of clinical trial, communication is the key for every trial study team and the stakeholders involved in the research. We communicate with researchers and investigators who collaborate with us efficiently via call or email. They will be informed about the email communication with trial participants, their consent forms, log-in information, etc., so they know about the progress of the clinical study.

Experienced Clinical Research Team

The whole journey of a clinical trial is not easy. You need the collaboration and assistance of multiple people. At Central Health Solutions, we have an experienced clinical research team to provide support during clinical trials. Their experience allows them to take care of every aspect of the clinical trial journey. They will ensure your study progresses in a smooth and efficient way and you see outstanding results in your study. Our team includes: