01 · PDRI®
What is PDRI®?
PDRI® (Project Definition Rating Index) is a structured tool used during front end planning to assess the completeness of project scope definition. It helps teams identify gaps and project risk factors before detailed design and construction.
The index was developed by the Construction Industry Institute in the USA and The University of Texas at Austin. Individual PDRI® publications relate to various sectors – mining, civil engineering, industrial construction and infrastructure.
The traditional PDRI® for industrial projects uses a 0–1000 point scale. The lower the score, the better defined the project.
Back to contents ↑How to Interpret a PDRI® Score
As practical indicative ranges:
PDRI® scoreAssessmentMeaning
0–200Very well definedStrong level of project definition; an important benchmark before detailed design / execution.
201–300Well definedMinor to moderate gaps; generally suitable for progression once critical actions are closed.
301–400Moderate definitionSignificant gaps remain and should be addressed before proceeding.
401–500Poor definitionSignificant uncertainty; additional front-end planning is recommended.
>500Poorly definedMajor unresolved issues; proceeding creates substantial project risk.
Important: these are practical interpretive ranges, not universal CII thresholds for every PDRI® application. The score should always be interpreted in relation to project type, project phase and the specific PDRI® version being used.
For CII small industrial projects, the typical early-review range is 400–800, while the final review typically falls within 150–400, with a target of 300 or below.
For large and complex industrial projects, 200 points is a particularly important benchmark. CII research found that projects scoring below 200 generally performed better in terms of cost, schedule and change performance.
Back to contents ↑How to Assess Project Readiness
Project readiness should cover more than the completeness of engineering documentation. It should also consider:
- project scope and boundaries,
- technical and process requirements,
- project input data,
- site conditions,
- technical concept,
- legal and permitting requirements,
- procurement and execution strategy,
- schedule and budget,
- project organization,
- risks and project assumptions.
PDRI® converts this assessment into a structured and measurable process, identifying gaps that need to be addressed before moving to the next project phase.
Back to contents ↑PDRI® and Project Readiness for Execution
PDRI® is a key tool for assessing Project Readiness, but the score should not be the sole basis for an execution decision. As a practical interpretation:
- PDRI® ≤200 – the project is well defined and may be considered ready for progression, subject to closing critical actions.
- PDRI® 200–300 – the project is generally well prepared, but remaining gaps and their risk impact should be reviewed.
- PDRI® 300–400 – additional work is required to strengthen project definition and close key gaps.
- PDRI® >400 – caution is recommended before committing to major execution activities; critical definition gaps should be addressed first.
PDRI® does not simply answer “Can we start the project?” It answers “How well is the project defined, and where are its weaknesses?”
Back to contents ↑02 · Project Management
Causes of EPC Project Delays
EPC project delays rarely have a single cause. They are usually the result of problems accumulating from the early stages of the project.
Typical causes include:
- incomplete project definition,
- scope and client requirement changes,
- engineering and document approval delays,
- design errors and inconsistencies,
- long-lead procurement problems,
- supplier and subcontractor delays,
- poor multidisciplinary coordination,
- slow decision-making,
- ineffective information flow,
- inadequate planning and control.
Delays often develop as a chain reaction: Decision → Engineering → Procurement → Construction. Effective delay management therefore requires identifying the root cause, rather than simply monitoring the resulting delay.
Back to contents ↑Project Recovery Plans
A Project Recovery Plan is a structured set of actions designed to restore control over scope, schedule, cost and resources.
A good recovery plan should answer:
- What went wrong? – identify causes and impacts.
- Where are we now? – assess the current project status.
- What needs to change? – define corrective actions, priorities and resources.
- How will we recover the schedule? – establish a realistic recovery programme and focus on the critical path.
A recovery plan should not simply be a revised schedule. It should define how the project will be managed differently.
Back to contents ↑Risk Management
Risk management is more than maintaining a Risk Register. Its purpose is to reduce both the probability and impact of events that could negatively affect project objectives.
The process includes:
- risk identification,
- probability and impact assessment,
- risk ownership,
- preventive and mitigation actions,
- trend monitoring,
- contingency planning,
- regular risk profile updates.
Mature risk management means moving from “What are our risks?” to “What are we doing to prevent the risk from becoming a problem?”
Back to contents ↑Project Control Indicators
Project Controls provide the information needed to determine whether the project is progressing towards its objectives.
Key areas include:
- Schedule – programme and progress,
- Cost – budget and cost forecast,
- Engineering – documentation and approvals,
- Procurement – orders and deliveries,
- Construction – physical progress,
- Changes – scope changes,
- Risks – risk levels and trends,
- Cash Flow – actual and forecast cash inflows and outflows.
Good KPIs should not only show what has happened, but also indicate what is likely to happen next.
Back to contents ↑03 · Supply Management
How to Evaluate an Equipment Supplier
Supplier evaluation should go beyond price. Key criteria include:
- experience and references,
- technical competence,
- manufacturing capacity,
- quality management,
- inspection and testing capabilities,
- personnel qualifications,
- financial stability,
- availability of materials and components,
- international delivery experience,
- ability to meet the required schedule.
The best supplier is not necessarily the cheapest supplier. It is the supplier capable of reliably meeting technical, quality and schedule requirements.
Back to contents ↑Technical Bid Evaluation
Technical Bid Evaluation (TBE) is used to compare supplier offers against project requirements.
The assessment should cover:
- datasheet and specification compliance,
- materials,
- technical parameters,
- applicable standards,
- scope of supply,
- certificates and documentation,
- inspection and testing,
- technical warranties,
- deviations,
- installation and commissioning requirements.
A good TBE should identify not only technical compliance, but also the risks associated with selecting each supplier.
Back to contents ↑Supplier Evaluation
Supplier evaluation should be performed before selection, during execution and after delivery.
Before placing an order, the evaluation should cover the supplier’s experience, quality performance, technical capability, manufacturing capacity and financial stability.
During execution, key areas include:
- manufacturing progress,
- documentation,
- quality,
- inspections,
- schedule,
- material procurement,
- corrective actions,
- readiness for shipment.
After delivery, performance can be assessed against: Quality – Delivery – Cost – Technical Performance – Documentation.
Back to contents ↑Sourcing of Specialized Equipment
The sourcing process should include:
- defining requirements,
- identifying technologies and manufacturers,
- developing a long list,
- verifying capabilities,
- developing a short list,
- issuing RFQs,
- technical and commercial evaluation,
- supplier audit or inspection,
- negotiations,
- supplier recommendation.
For custom-made, long-lead or technically high-risk equipment, sourcing should start as early as possible.
The objective is not to find the cheapest manufacturer, but the supplier capable of delivering the right technology, quality and schedule at an acceptable level of risk.
Back to contents ↑04 · Engineering & Design
FEED vs. Basic Design
FEED (Front-End Engineering Design) establishes the main technical solutions, project scope, process parameters, major equipment requirements and key cost and schedule assumptions.
Basic Design further develops these assumptions to support detailed engineering, procurement and construction.
Key elements include:
- project scope and boundaries,
- design basis,
- material and energy balances,
- process parameters,
- process concept,
- major equipment requirements,
- infrastructure,
- applicable codes and standards,
- cost and schedule assumptions.
A well-developed FEED reduces uncertainty and provides a sound basis for investment decisions.
Back to contents ↑Constructability / Feasibility Assessment
A Constructability / Feasibility Assessment determines whether the proposed design can actually be executed under the assumed project conditions.
It may cover:
- equipment transportation,
- site access,
- cranes and lifting equipment,
- installation of heavy equipment,
- existing infrastructure,
- site conditions,
- construction sequence,
- work within operating facilities,
- safety,
- availability of contractors and materials,
- site constraints,
- required execution schedule.
A technically correct design is not necessarily a design that can be constructed efficiently and economically.
Back to contents ↑Technical Assessments
A Technical Assessment is an independent review of a technical solution, equipment item or engineering package against project requirements.
It may include:
- verification of design assumptions,
- process solution assessment,
- documentation review,
- materials assessment,
- code and standard compliance,
- equipment and supplier evaluation,
- identification of errors and inconsistencies,
- interface review,
- technical risk assessment,
- optimization recommendations.
The purpose is not simply to identify errors, but to confirm that the proposed solution is technically appropriate, feasible, safe and fit for purpose.
Back to contents ↑05 · Quality
HACCP
HACCP (Hazard Analysis and Critical Control Points) is a key food safety management system; its implementation is a legal requirement for every business operating in the food industry.
This system is based on 7 core principles that ensure the product reaching the consumer is completely safe for their health:
- Hazard analysis – identifying potential dangers (e.g., bacteria, foreign objects).
- Determination of Critical Control Points (CCP) – identifying stages in the process where a hazard can be controlled.
- Establishment of critical limits – setting clear boundaries (e.g., maximum storage temperature).
- Establishment of a CCP monitoring system – regularly checking and measuring parameters at these points.
- Determination of corrective actions – planning the steps to be taken if standards are exceeded.
- Establishment of verification procedures – confirming, through testing methods, that the system is functioning correctly.
- Maintenance of documentation – meticulously recording all actions and measurements.
Implementing an HACCP system minimizes the risk of product loss, protects the brand from reputational crises, and demonstrates that you prioritize consumer safety.
Back to contents ↑GHP and GMP
GHP (Good Hygiene Practice) and GMP (Good Manufacturing Practice) are sets of principles that define how to conduct operations in the food industry, step by step, to ensure that every product is completely safe.
GMP (Good Manufacturing Practice) – requirements concerning the production environment and technology. They include, among other things:
- Location and infrastructure – an appropriate layout of premises to prevent cross-contamination.
- Technical condition of machinery – regular servicing, certifications, and proper use of equipment.
- Quality of raw materials – supplier oversight and proper storage of ingredients.
GHP (Good Hygiene Practice) – requirements focused directly on cleanliness and sanitary procedures. They include, among other things:
- Personnel hygiene – clean protective clothing, handwashing, training, and the health status of employees.
- Cleaning and disinfection – rigorous plans for maintaining the cleanliness of premises and equipment.
- Waste management – safe disposal of waste and pest control measures (DDD – disinfection, disinfestation and deratization).
These two practices eliminate most day-to-day sanitary risks even before a formal HACCP plan is established. For your company, this ensures trouble-free inspections by sanitary authorities, reduces the risk of material losses, and guarantees that your staff operates according to the highest hygiene standards on the market.
Back to contents ↑Quality Tools
Quality management tools allow for the precise identification of the source of a problem and help effectively prevent its recurrence. The most commonly used quality tools in modern business include:
- Ishikawa diagram (cause-and-effect diagram) – used to graphically represent and analyze all potential causes of a given problem. It helps teams think outside the box and group sources of errors into key categories, such as: man, machine, material, method, measurement, and environment.
- Pareto-Lorenz chart (80/20 rule) – a statistical tool based on the principle that 20% of causes generate 80% of problems. It allows a company to quickly rank errors from most to least significant, enabling them to focus their efforts and budget on addressing those that will yield the greatest return.
- Flowchart (process map) – a visual map of a process that illustrates every step of production or service delivery using standardized symbols. It makes it easy to identify bottlenecks, redundant operations, and areas where errors occur most frequently.
- Check sheet (checklist) – a simple yet highly powerful form used for the systematic collection of data in real time. It allows employees to quickly mark off completed tasks or record the frequency of specific defects, creating a clear dataset for further analysis.
- Histogram – a bar chart that displays the frequency distribution of data (e.g., product dimensions or service lead times). It reveals the central tendency and variability of a process, making it easier to assess whether the process is stable and remains within tolerance limits.
Implementing traditional quality tools marks a shift from reactive “firefighting” to proactive business management. Utilizing these methods enables process optimization in the spirit of Lean / Six Sigma. For your organization, this means less waste, higher team efficiency, complete product consistency, and a significant boost in end-customer satisfaction.
Back to contents ↑Quality Audit
A quality audit is a systematic, independent, and documented examination designed to evaluate whether quality-related activities and their outcomes align with planned arrangements and standards.
An audit is not a means of “assigning blame” or a form of policing; rather, it is a strategic diagnostic tool. Its primary purpose is to provide objective confirmation that a company’s processes are functioning correctly, while also identifying areas that require optimization or corrective action to meet customer requirements and established standards.
To ensure an audit delivers maximum value to an organization, it must be precisely tailored to its intended objective. Classification by the auditing party (who is conducting the audit?):
- First-party audit (internal audit) – conducted by an organization for its own purposes. Designated, trained staff members (internal auditors) verify the company’s own processes to ensure the system is operating effectively, procedures are being followed, and the organization is prepared for external inspections.
- Second-party audit (supplier/customer audit) – conducted by a company at the premises of its existing or potential suppliers and subcontractors (or, conversely, by a customer at your company). It is used to assess whether a business partner meets contractual requirements, maintains stable processes, and can guarantee reliable, consistent, and safe deliveries.
- Third-party audit (certification/external audit) – performed by a completely independent, accredited certification body (e.g., TÜV, SGS). Its purpose is to provide an objective confirmation that a system complies with an international standard (e.g., ISO 9001, IATF 16949), culminating in the issuance of an official certificate.
Classification by audit subject (what is being audited?):
- System audit – evaluates the organization’s overall quality management system (including documentation, quality policy, management commitment, and the achievement of business objectives).
- Process audit – focuses on a specific technological or operational sequence (e.g., welding, packaging, or complaint handling), verifying its stability and adherence to established instructions.
- Product (or service) audit – assesses the final output against technical specifications and customer requirements, often through a detailed examination of randomly selected finished goods.
A professionally conducted quality audit is the best investment in the stability and growth of any enterprise. Rather than reacting to errors after they occur, an audit allows for the early detection of risks. Whether you require an internal audit in preparation for a regulatory inspection (such as one by sanitary authorities), a supplier audit to secure your supply chain, or support with ISO certification, quality audits provide you with full control over your processes, minimize the costs associated with poor quality, and enhance your brand’s market prestige.
Back to contents ↑Training
Professional quality training – invest in knowledge that eliminates errors. Transform quality management theory into tangible profits for your company.
We offer practical training designed for management, engineers, and frontline staff who want to effectively optimize processes and eliminate the costs of poor quality. Our programs combine solid theoretical knowledge with hands-on workshops (case studies), providing participants with ready-to-use tools that can be implemented immediately.
Our training areas include:
- Safety and quality systems: HACCP, GHP, GMP, and ISO standard requirements (e.g., ISO 9001).
- Quality tools in practice: practical workshops covering the Ishikawa diagram, Pareto analysis, 5W2H, and Lean / Six Sigma methodologies.
- Auditor Academy: preparation for the role of an internal auditor (first-party audit) or a supplier auditor (second-party audit).
- Cost of Quality (COQ) optimization: how to measure, analyze, and effectively reduce quality-related costs within an organization.
- A practical approach: no boring lectures – we focus on real-world challenges specific to your industry.
Back to contents ↑