Guidelines, SOPs & templates

Everything you need to prepare a sound submission: downloadable templates, standard operating procedures, role permissions, and the correspondence policy.

Downloadable templates:
FORM

Human protocol form

IRB study structure & requirements — fill in & export PDF.

Open form →
FORM

Animal protocol form

IACUC protocol & 3Rs justification — fill in & export PDF.

Open form →
FORM

Informed consent form

Participant consent document — fill in & export PDF.

Open form →
FORM

PI declaration

Signed responsibility & compliance — fill in & export PDF.

Open form →
FORM

Adverse-event report

For use during continuing review — fill in & export PDF.

Open form →
FORM

Amendment/renewal

Modify or extend an approval — fill in & export PDF.

Open form →

All forms above are completed online, then exported as PDF, signed, and uploaded with your submission.

Additional approval required

Does your study also need Ministry of Health approval?

Research carried out within, or in collaboration with, Ministry of Health facilities — or involving MoH patients, staff, data, or samples — requires an additional approval from the National Center for Training and Human Development before it can proceed. Download the application form below and review the Ministry's research priorities.

Sample-size calculator


Estimate the minimum sample size for your study design. Choose the type, enter your expected values, then press Calculate sample size. Formulas are taken from peer-reviewed methodological references (see the citation below the tool) and should be confirmed with a statistician at final planning.

For estimating a single proportion (e.g. a prevalence) in a descriptive or cross-sectional study.

Tip: If you don't know the expected proportion, use 50% — it gives the largest (most conservative) sample. Only enter a population size if it is finite and known (e.g. staff of one department); the finite-population correction is then applied.

Methodological reference for the calculation

Formulas are based on: Charan J, Biswas T. How to calculate sample size for different study designs in medical research? Indian J Psychol Med. 2013;35(2):121–126. doi:10.4103/0253-7176.116232. Supported by Cochran (Sampling Techniques, 1977), Pocock (Clinical Trials, 1983) and Hulley et al. (Designing Clinical Research, 2013).

How to cite this tool

When referring to this tool in your protocol or methods, use:

Research Ethics Committee, Polytechnic College of Karbala. Sample-size calculator. rec-pck.org/guidelines.html (accessed ).

How the committee operates?


  • SOP-01

    Submission intake & screening

    Completeness checks, panel routing, clock-pause rules.

  • SOP-02

    Reviewer assignment & COI

    Conflict flagging, reviewer blinding, recusal.

  • SOP-03

    Meetings & quorum

    Domain-specific quorum and minute-taking.

  • SOP-04

    Decisions & certificates

    Letterheads, decision letters, certificate issuance.

  • SOP-05

    Continuing review & inspection

    Reminders, amendments, semi-annual facility inspection.

  • SOP-06

    Archiving & audit log

    Read-only retention and action-log integrity.

Role-based access


RoleAccess rights
Submitter (ATU only)Create/edit own applications before submission, upload files, view own status, respond to revisions, download own approvals; no access to others' applications
REC secretaryView all applications, screen completeness, route to panels, manage calendars and reminders, issue letters/certificates, manage archive; cannot vote
Panel coordinatorAll Secretary view rights for own panel, assign reviewers, manage meetings, record decisions for own panel
ReviewerView only assigned applications, submit checklist and recommendation; cannot see other reviewers' identities (blinded) until decision
Veterinarian/LaypersonSame as reviewer, but flagged as mandatory for their protocol type
REC chair (head)Full read access across both panels, override/arbitration rights, sign final approvals, view audit logs and reports
System administratorTechnical access: user management, domain-restriction settings, backups, audit-log integrity; no review or voting role

Email handling policy:


A single authenticated address:

All official correspondence (confirmations, decisions, certificates, reminders) is sent from one authenticated system address, no-reply@rec-pck.org, with rec.pck@atu.edu.iq as the monitored reply-to for queries.

Not sent from users' mailboxes:

Official committee mail is not sent from individual @atu.edu.iq mailboxes, that breaks the audit trail and can't be authenticated. Instead, every action is logged to the named user inside the system, and notifications are addressed to their verified inbox but sent from the rec-pck.org address.