Conceptual Design

The first step in any successful project is Conceptual Engineering. This phase focuses on defining the project's scope, feasibility, and high-level design, ensuring that all requirements are clearly understood and mapped out.

What We Deliver:

Project feasibility analysis and risk assessment

Preliminary facility layout and space planning

Initial process flow diagrams (PFDs)

High-level cost estimates and budget planning

Regulatory and compliance considerations (GMP, FDA, ISO)

Regulatory and compliance considerations (GMP, FDA, ISO)

Basic and Detailed Engineering

Detailed Engineering is where we finalize every aspect of the project, providing precise, actionable designs that guide construction, installation, and system validation.

What We Deliver:

HVSC Design

Room layout with machine GA positioning(Process + Utility equipment)

Site master planning

EMS AND BMS

Process engineering

Environmental engineering

Civil & Structural scope

Utility engineering

Clean Utility System

Piping engineering (insulation and painting of pipes)

Electrical Engineering

Firefighting system

BOM AND BOQ COMPILATION

Drawing and specifications including Architectural scope Drain point layout

Epoxy flooring finishing layout

Wall finishing layout

Hazardous classification layout

Emergency escape layout

Utility consumption sheet

Equipment load and Power consumption sheet

Facility Civil and Structural Evolution and Engineering

Basic Engineering

In the Basic Engineering phase, we transform the initial concept into a more defined project plan. We develop key designs and technical specifications that guide the procurement and construction phases.

What We Deliver:

Process flow diagrams (PFDs) and piping & instrumentation diagrams (P&IDs)

Preliminary equipment sizing and technical specifications

Basic facility layouts, including cleanroom zoning

Initial timelines and cost estimates for construction and materials

Early-stage regulatory compliance strategy (GMP, FDA, ISO alignment)

Regulatory and compliance considerations (GMP, FDA, ISO)

HVAC Systems for Controlled Environments

Our customized HVAC systems are designed specifically for pharmaceutical environments, ensuring precise control over temperature, humidity, and air quality. We develop energy-efficient systems that maintain sterility and compliance in cleanroom settings.

What We Deliver:

Custom HVAC system design for pharmaceutical environments

Temperature and humidity control

Cleanroom filtration systems (HEPA/ULPA)

Real-time environmental monitoring

Energy-efficient and sustainable solutions

Cleanroom Design

Cleanrooms are critical to pharmaceutical production. We specialize in designing cleanrooms that meet your specific operational requirements, ensuring compliance with ISO standards and stringent regulatory guidelines. Our cleanrooms are modular, flexible, and scalable, allowing for future upgrades.

What We Deliver:

ISO Class 5 to Class 8 cleanroom designs

Modular and flexible construction

Custom airflow systems (laminar flow, unidirectional flow)

HEPA/ULPA filtration integration

Compliance with ISO 14644 and GMP standards

Process Equipment Integration

From conceptual design to full integration, we handle the design, installation, and validation of process equipment, ensuring seamless operations and regulatory compliance. 

What We Deliver:

Custom equipment design and installation

Integrated process automation systems

Aseptic processing equipment design

Utility systems (purified water, steam, compressed air)

Process control systems for real-time monitoring

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Where sustainability meets reliability and performance.

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Where sustainability meets reliability and performance.

connect with us