Greenfield Pharma Project Design and Consulting

At Magnificent Concept, we believe that every successful project starts with a smart concept. By engaging with us early in your project lifecycle, we help you uncover opportunities to enhance system performance and optimize your investment.

With our in-depth experience in planning and setting up pharmaceutical facilities, we transform ideas into well-structured, regulation-ready projects. Our strong global network including collaborations with international consultants, regulatory authorities, and industry bodies keeps us at the forefront of pharma engineering standards.

We begin with a clear understanding of your production goals, automation needs, dosage forms, equipment requirements, and compliance levels. Based on this, we deliver:

• Preliminary plant layout designs

• Equipment sizing and basic technical specifications

• Environmental classifications and pressure differential mapping

• Water treatment system concepts

• Civil construction scope

• Preliminary project costing

• Tentative project timelines

Our mission: to provide smart, efficient, and regulatory-compliant design solutions that never compromise on quality.

Basic Engineering Design

We develop tailored basic engineering packages that align with your functional goals and site-specific needs always adhering to current GMP norms and international standards.

Our Basic Engineering Services include:

• Multiple layout options aligned with GMP standards.

• Initial HVAC and pressure differential system concepts with air flow diagrams.

• Optimized personnel and material movement drawings.

• Utility system concepts for purified water, steam, gases, solvents, and more.

• P&ID diagrams for key processes and utilities.

• Preliminary electrical load calculations.

• Conceptual plan for effluent treatment (ETP).

Detailed Engineering

Our detailed engineering services bridge the gap between planning and construction, ensuring every component is optimized for performance, compliance, and budget. This phase focuses on cross-disciplinary coordination to accelerate commissioning and reduce execution delays.

We offer in-depth engineering across the following disciplines:

• Civil & Structural Design

• Architecture & Space Optimization

• Process Engineering & Equipment Selection

• Mechanical & Piping Design

• Plumbing & Drainage Layout

• Electrical Systems Planning

• HVAC and Cleanroom Environment Design

• Instrumentation Schematics

• ETP System Layout

• Laboratory Furniture Design & Specification

Procurement Support

With our industry relationships and procurement experience, we help you acquire the right machinery and systems at the best value without compromising on quality.

Our procurement support includes:

• Drafting technical tender documents for key systems (HVAC, water, electrical, steam, etc.)

• Bid evaluation and vendor selection based on technical and commercial merit

• Preparation of equipment specifications and detailed datasheets

• Review and approval of vendor technical drawings

• Coordination with vendors to ensure timely delivery

Project Coordination & Execution Management

Our project management services are built to keep your vision on track ensuring transparency, timeline adherence, and streamlined execution.

We manage the full project lifecycle with:

• Customized project procedures and communication frameworks

• Timeline and work schedule development (Gantt/Bar Charts)

• Progress tracking for engineering, procurement, and construction phases

• Regular coordination meetings with stakeholders

• Tentative cost tracking during detailed design phase

• Document control systems to maintain version integrity at site

Greenfield Pharma Project

At Magnificent Concept, we specialize in transforming ideas into world-class pharmaceutical manufacturing facilities through our expertise in Greenfield Projects. A Greenfield project refers to constructing a brand-new,purpose-built pharmaceutical plant from the ground up, on previously undeveloped land offering complete design flexibility, regulatory compliance, and future-ready scalability.

Our Approach

1. Site Selection and Feasibility Studies

Success begins with selecting the right location. We perform detailed site assessments considering environmental impact, regulatory requirements, utility availability, logistics connectivity, and long-term operational sustainability. Our feasibility studies evaluate technical, financial, and regulatory viability before any major investment is made.

2. Conceptual Design and Master Planning

We work hand-in-hand with clients to understand project goals and transform them into innovative yet practical designs. Our conceptual designs prioritize regulatory compliance (GMP, USFDA, MHRA, EU-GMP), process flow optimization, personnel and material movement, energy efficiency, and future scalability.

3. Detailed Engineering and Compliance Strategy

Our engineering team develops complete architectural, civil, structural, MEP (Mechanical, Electrical, Plumbing), and HVAC designs aligned with pharmaceutical industry standards. We ensure early-stage integration of validation, quality assurance, and regulatory compliance into every aspect of the design.

4.Commissioning, Qualification, and Validation (CQV)

Before handover, we undertake a rigorous CQV process to ensure every utility, system, and process meets predefined acceptance criteria. We prepare complete documentation required for regulatory inspections and support our clients in achieving rapid facility approval.

5. Operational Readiness and Handover

We provide complete support for facility operational readiness — including SOP preparation, staff training, and system integration — to ensure a seamless transition from project completion to commercial manufacturing operations.