Looking for independent medical research guidelines? Celerion is committed to providing absolute transparency as one of the world's premier clinical research organizations (CROs). Below is a curated directory of external regulatory bodies, ethical codes, and independent watchdogs that oversee global health safety protocols across all phases of clinical trials.

AAHRPP

http://www.aahrpp.org/

The Center for Information and Study on Clinical Research Participation (CISCRP)

https://www.ciscrp.org/

Clinical Trials.gov

http://www.clinicaltrials.gov/

FDA (Food & Drug Administration)

http://www.fda.gov/

OHRP (Office for Human Research Protections)

http://www.hhs.gov/ohrp/

Ethical Principles and Codes

The Belmont Report: Ethical Principles and Guidelines for the Protection of Human Research Subjects

http://ohsr.od.nih.gov/guidelines/belmont.html

The Nuremberg Code: Directives for Human Experimentation

http://ohsr.od.nih.gov/guidelines/nuremberg.html

World Medical Association Declaration of Helsinki: Ethical Principles for Medical Research Involving Human Subjects

https://www.wma.net/policies-post/wma-declaration-of-helsinki-ethical-principles-for-medical-research-involving-human-subjects/

Have more questions about our regulatory standards? These independent resources demonstrate the rigorous frameworks that guide every study. If you want to learn more about how Celerion enforces these protections as a fully certified clinical research organization, please review our FAQ panel or contact our study coordinators. We want you to feel completely safe and confident before volunteering for our upcoming clinical trials.