Blog
Guides for volunteers, CROs and sponsors taking part in clinical trials in India and beyond.
21 October 2026 ยท 3 min read
Understand how clinical trials work, how they differ from observational studies, and what to ask about eligibility, consent and safety before joining.
Read article โ21 October 2026 ยท 3 min read
A plain-language guide to clinical trial phases: what each phase investigates, who may participate and why a phase number does not guarantee safety or benefit.
Read article โ21 October 2026 ยท 3 min read
Find clinical trials by condition and location on ClinicalTrials.gov, then check recruitment status, eligibility, contacts and results before approaching a study team.
Read article โ21 October 2026 ยท 3 min read
Learn what a clinical study report contains, how ICH E3 organises methods and results, and what CROs and sponsors should review before finalising a CSR.
Read article โ1 October 2026 ยท 5 min read
What every clinical trial volunteer in India should know about informed consent, who can see their personal data, compensation, and how to withdraw from a study.
Read article โ26 September 2026 ยท 6 min read
What sponsors should check before awarding a study to an Indian CRO: certifications, study volume, therapeutic experience and verified directory profiles.
Read article โ20 September 2026 ยท 4 min read
Eligibility matching, de-identified candidate previews and per-candidate unlocks: how modern CRO recruitment cuts screening time while keeping volunteer data protected.
Read article โ12 September 2026 ยท 5 min read
How a verified volunteer passport helps healthy participants move between BA/BE studies safely, with dosing history, washout tracking and consent records in one place.
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