ISO 17021 Advisory
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Consultancy Capabilities

End-to-End Management System Consultancy & Audit Preparation

We guide organizations across India and international markets from initial clause diagnosis to third-party certification audit confidence. Learn how our 5 consultancy pillars deliver verifiable operational results.

The 5 Consultancy Pillars

How Proceva Delivers Management Excellence

Our structured, hands-on advisory framework is built around five rigorous operational phases.

01
Phase One

Diagnostic Gap Analysis

We conduct a comprehensive diagnostic review of your ongoing operational practices against the mandatory clauses of your target ISO standard. Rather than assuming everything needs replacement, we honor what already works and document precise compliance deficiencies.

Clause-by-Clause Evaluation

Deliverables & Methodology:

  • Baseline Compliance Matrix: Explicit clause-by-clause grading (Conforming, Partially Conforming, Absent).
  • Implementation Milestone Schedule: Realistic calendar matching your team's bandwidth and commercial deadlines.
  • Resource & Responsibility Matrix: Designating departmental champions and process owners early.
02
Phase Two

Pragmatic SOP & Manual Development

We eliminate excessive paperwork. Our consultants author concise, functional Standard Operating Procedures (SOPs), Work Instructions, Policy Statements, and Risk & Opportunity registers that reflect your real operational tools (ERP, Excel, emails).

Lean Documentation

Deliverables & Methodology:

  • Quality / Integrated Management Manual: High-level policy document articulating scope and leadership commitment.
  • Departmental SOPs & Flowcharts: Practical step-by-step procedures for procurement, production, QA, sales, and HR.
  • Risk & Opportunity Register (Clause 6.1): Actionable risk mitigation logs customized to your market risks.
03
Phase Three

Process Implementation & Workforce Coaching

A management system must live in the routines of your workforce. We conduct departmental sensitization sessions, teach operators and supervisors how to log non-conformances, calibrate gauges, and maintain verifiable records.

Interactive Training

Deliverables & Methodology:

  • Hands-On Workshop Modules: Tailored training sessions for supervisors, engineers, and office staff.
  • KPI Tracking & Quality Objectives: Establishing measurable departmental goals (Clause 6.2).
  • Record-Keeping Routine Verification: Periodic monitoring to ensure logs are actively filled out.
04
Phase Four

Rigorous Internal Audits & MRM

Before any third-party auditor visits your site, Proceva conducts a rigorous internal audit simulation. We interview process owners, sample records, raise simulated Non-Conformances (NCs), and conduct the formal Management Review Meeting (MRM).

Audit Simulation

Deliverables & Methodology:

  • Formal Internal Audit Report: Detailed non-conformance logs categorized by severity (Major, Minor, Observation).
  • Root Cause Analysis & CAPA: 5-Why analysis and corrective action verification before the external audit.
  • Management Review Meeting (MRM) Minutes: Documented leadership review satisfying Clause 9.3 mandates.
05
Phase Five

Stage 1 & Stage 2 Audit Preparation & Support

We prepare your management and team to face the independent accredited Certification Body (CB) auditors with confidence. We review dossiers, coach staff on presenting evidence calmly, and help formulate formal CAPA closures for any audit findings.

Certification Body Readiness

Deliverables & Methodology:

  • Stage 1 Documentation Readiness Review: Ensuring manuals, policies, and internal audit records pass registrar desk audit.
  • Stage 2 On-Site / Remote Audit Handholding: Guiding your team on answering auditor inquiries accurately.
  • NC Closure Dossier: Assisting in resolving minor audit observations and submitting validated closure evidence.
Individual Standards

Dedicated Consultancy for Global Standards

Explore our specialized advisory pages for individual standards or integrated management frameworks.

ISO 9001:20154-8 wks

Quality Management Systems (QMS)

The global benchmark for quality management. We help you design lean processes that enhance customer satisfaction, reduce rework, streamline vendor control, and satisfy enterprise vendor evaluation criteria.

Explore Standard Requirements
ISO 14001:20156-10 wks

Environmental Management Systems (EMS)

A structured framework to manage environmental risks, optimize waste and energy consumption, ensure strict statutory compliance with pollution boards, and fulfill international ESG supplier expectations.

Explore Standard Requirements
ISO 45001:20186-10 wks

Occupational Health and Safety (OH&SMS)

The premier international standard for workplace safety. We help you establish hazard identification, risk assessment (HIRA), incident reporting mechanisms, and employee safety participation.

Explore Standard Requirements
ISO 27001:20228-14 wks

Information Security Management Systems (ISMS)

The definitive global standard for cybersecurity, data governance, and risk mitigation. We guide tech organizations and data-handling enterprises through Statement of Applicability (SoA) and Annex A controls.

Explore Standard Requirements
Integrated Management Systems8-12 wks

Integrated Management Systems (IMS: 9001 + 14001 + 45001)

Why maintain three separate manuals and manage three isolated audit cycles? We harmonize ISO 9001, 14001, and 45001 under the High-Level Structure (Annex SL), uniting shared clauses across quality, environment, and occupational safety into a single, efficient operational system.

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ISO 22000:2018 & HACCP6-10 wks

Food Safety Management Systems (FSMS)

Comprehensive food safety management combining prerequisite programs (PRPs), hazard analysis critical control points (HACCP), and traceability systems for domestic compliance and food exports.

Explore Standard Requirements
Confidential Assessment • Senior Auditor Review

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