
ISO 9001:2015 (QMS)
Consistent product/service quality, defined processes, NCR/CAPA discipline and measurable KPIs.
End-to-end documentation, trainings, internal audits, readiness, and coordination with accredited certification bodies.
Documentation → Training → Internal Audit → Readiness → External Audit Coordination.
Consistent product/service quality, defined processes, NCR/CAPA discipline and measurable KPIs.
Aspect/impact registers, legal register, objectives & programs to improve environmental performance.
Hazard identification, risk assessment, incident investigation—build a strong safety culture.
Food safety plans, PRPs, CCPs and end-to-end traceability across the supply chain.
ISMS scope, risk assessment, Annex A controls, SoA, and BC/DR for robust data security.
Energy baseline, EnPIs, and opportunity register—reduce costs while advancing sustainability.
Risk-based QMS, design control, sterile controls—global acceptance for medical devices.
Capability maturity, measurement & analysis, engineering/PM practices for predictability and quality.
We don’t just write documents—we operationalize them so audits are smooth and the system scales.
Ready-to-use SOPs, registers, trackers, and dashboards.
Internal audits, CAPA closure, and external audit day support.
Milestone-based plan, weekly cadence, and clear ownership.
Transparent pricing with no hidden fees.
Discovery → Gap → Implementation → Internal Audit → Readiness → Certification.
Understand scope, sites, headcount, customer and regulatory needs.
Clause-wise mapping of AS-IS vs. standard; form the action plan.
Policies, SOPs, records, training, risk & objectives rollout.
Internal audit, MRM, CAPA, and coordination with certification body.
Quick answers to common questions.
Share your scope—we’ll send a 90-day roadmap and a fixed quote.