Ethics and do no harm
Informed consent, voluntary participation, confidentiality, respectful engagement, appropriate referral considerations and risk-sensitive methods.
Gesem integrates methodological rigour, participant protection, data quality and transparent review throughout the evidence cycle. The exact controls are adapted to the risk, population, method and client requirements of each assignment.
Collect only what is needed, protect people and information, document decisions, check quality early, and communicate limitations clearly.
These commitments provide a consistent quality logic while allowing project-specific protocols to reflect the context and client requirements.
Informed consent, voluntary participation, confidentiality, respectful engagement, appropriate referral considerations and risk-sensitive methods.
Tool testing, validation rules, training, supervision, daily review, cleaning logic, version control and documentation of analytical decisions.
Collection limited to assignment needs, controlled access, secure handling practices and appropriate treatment of identifying or sensitive information.
Use of multiple sources and methods where appropriate, senior review, contradiction checks, limitation analysis and validation of key interpretations.
Clarify use, questions, indicators, sample logic, inclusion needs, ethical risks, data flows, analysis requirements and decision points.
Review wording, translation needs, skip logic, response options, measurement consistency, field usability and digital constraints.
Build shared interpretation of tools, consent, probing, safeguarding, field procedures and escalation paths; refine instruments before scale-up.
Monitor progress, completeness, duration, patterns, GPS or other permitted checks, qualitative depth and emerging operational risks.
Document cleaning, coding and assumptions; test consistency; examine disaggregation; triangulate sources; separate evidence from interpretation.
Use clear evidence chains, acknowledge limitations, distinguish findings from recommendations and check alignment with TOR questions and deliverables.
Research involving children, displaced people, conflict-affected communities, protection concerns or sensitive personal information requires stronger safeguards than routine organisational consultation.
Where relevant, Gesem works with the client to clarify required ethical approvals, safeguarding protocols, consent and assent arrangements, referral pathways, data-access restrictions and secure transfer or retention requirements. Requirements that depend on a client, funder or ethics body are agreed before implementation rather than assumed.
Gesem does not publish sensitive corporate files openly, but qualified clients and partners can request relevant credentials during an RFQ, vendor-onboarding, consortium or contracting process.
Company profile, registration and current business-licence information, applicable tax documentation and other corporate records requested for legitimate procurement.
Assignment-specific CVs, selected references, completion evidence and relevant case-study information matched to the opportunity.
Ethics, consent, safeguarding, confidentiality, data-protection and field-quality requirements are documented at assignment level according to the TOR, client standards and participant risk.
Gesem will reflect them in the methodology, field procedures, staffing and quality-assurance plan.