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Customized Design Engineering

At Phed Pharma Solutions, we deliver customized design engineering services, guiding your projects from conceptual design to detailed engineering to ensure compliance, operational efficiency, and optimal performance. Whether you are building a new facility or upgrading an existing one, we provide the specialized engineering expertise you need to meet the highest regulatory standards.
Conceptual design blueprint for a pharmaceutical manufacturing facility."

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)

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)

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:

Final 3D facility layouts and detailed engineering drawings

Complete equipment lists and procurement plans

Detailed piping, electrical, and HVAC system designs

Comprehensive construction plans and schedules

Validation and qualification protocols (IQ/OQ/PQ)

Documentation for regulatory submission and approval

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.

Our Expertise:

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.

Our Cleanroom Solutions:

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 Offer:

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