Services

What We Do

At the Central Independent Ethics Committee (CIEC), our primary focus is to ensure that clinical research is conducted ethically, transparently, and with the utmost respect for the rights and safety of participants. We offer a comprehensive range of services designed to support researchers, sponsors, and institutions in meeting ethical and regulatory standards. With our multidisciplinary team of experts, we provide timely and thorough reviews, guidance, and ongoing oversight to ensure that every clinical trial adheres to the highest ethical principles.

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Our Core Ethical Services

Ensuring Ethical Excellence

Our multidisciplinary team offers comprehensive reviews, ongoing oversight, and expert guidance to protect the rights, safety, and well-being of all participants while supporting researchers in maintaining compliance with ethical and regulatory standards.

Ethical Review of Clinical Trial Protocols

Informed Consent Review

Continuous Monitoring and Oversight

Serious Adverse Event (SAE) Evaluation

Confidentiality and Data Privacy Safeguards

Review of Protocol Amendments

Our Features

Multidisciplinary Expertise

An Ethics Committee should be composed of a diverse group of professionals, including medical experts, scientists, legal advisors, and non-medical members. This ensures that the review process is well-rounded, considering various perspectives from both scientific and ethical standpoints. A balanced composition promotes unbiased decision-making.

Rigorous Ethical Review

The committee’s primary function is to rigorously review clinical trial protocols to ensure compliance with ethical standards and regulatory requirements. This includes assessing risks, evaluating the scientific merit of the research, and ensuring that the rights and safety of participants are prioritized throughout the study.

Protection of Participant Rights

A critical function of an Ethics Committee is to safeguard the rights, dignity, and welfare of participants. This includes ensuring that participants are fully informed about the trial’s risks and benefits, consent is obtained freely, and their privacy and confidentiality are maintained.

Ongoing Oversight and Monitoring

The Ethics Committee should provide continuous oversight of approved clinical trials. This includes monitoring compliance with the approved protocol, reviewing any amendments, and assessing serious adverse events (SAEs). Regular monitoring ensures that any ethical issues arising during the study are promptly addressed.

Commitment to Transparency and Accountability

Transparency in the committee’s decisions and processes builds trust among researchers, participants, and regulatory bodies. An Ethics Committee should provide clear communication about its reviews, decisions, and any conditions for approval, fostering accountability in clinical research.

Compliance with Regulatory Guidelines

An Ethics Committee must operate within the framework of national and international regulations, such as those set by the Central Drugs Standard Control Organization (CDSCO) and Schedule Y in India. Ensuring adherence to these legal requirements guarantees that clinical trials are conducted responsibly and in accordance with ethical norms.

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Reach Us

Location :

Gini Aria, A-703, S. No. 16/2/2A/1, Opposite to KJEI’s Trinity College, Kondhwa Annex, Pune, Maharashtra – 411048, India

Email :

info@centraliec.com

Phone :

+91 99751 67908

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