Pharma consultants and solution providers.
Strategic consulting partner for pharmaceutical organizations — delivering end-to-end solutions in facility design, regulatory compliance, GMP systems, audit readiness, and quality culture transformation.
Who We Are
We help pharmaceutical companies accelerate compliance, optimize operations, and achieve global regulatory readiness through practical, science-driven consulting.
Pharma Consulting Group (PCG) is a specialized pharmaceutical consulting firm delivering strategic, technical, and regulatory solutions across the life sciences industry.
We support pharmaceutical companies throughout the entire product lifecycle — from facility design and project execution to GMP compliance, regulatory inspections, and operational excellence.
Our team combines deep industry experience with regulatory expertise across WHO GMP, US FDA, EU GMP, PIC/S Guidelines, and ICH Standards to build sustainable quality systems and strengthen compliance.
To become a trusted global partner for pharmaceutical excellence, enabling healthcare organizations to deliver safe, effective, and high-quality medicines worldwide.
To empower pharmaceutical companies with innovative, practical, and compliant solutions that enhance product quality, regulatory compliance, and operational efficiency.
Our leadership team brings extensive experience in pharmaceutical quality systems, GMP compliance, regulatory audits, engineering projects, and operational excellence.
Our multidisciplinary team includes experts in Quality Assurance & Compliance, GMP Systems, Engineering & Facility Design, Validation, Audit Readiness, and Technology Transfer.
What We Do Best
Comprehensive GMP and quality management consulting to meet international regulatory standards.
Expert engineering solutions for facility design, utilities, clean rooms, and turnkey projects.
Thorough audits to assess compliance and actionable remediation strategies.
Seamless technology transfer from development to commercial production.
Customized training programs to boost operational capabilities and ensure continuous improvement.
Streamlining processes for efficiency, productivity improvements, and quality culture transformation.
Comprehensive documentation support for Quality Management Systems meeting regulatory standards.
Full qualification and validation services from equipment qualification to process validation.
Expert regulatory guidance to navigate complex global compliance requirements.
How We Help
We provide end-to-end consulting support to pharmaceutical companies across multiple domains.
Expert plant setup and design services adhering to international standards such as WHO, US FDA, EU GMP and other regulatory requirements. Whether it's a new facility or an expansion, our designs ensure compliance, efficiency, and sustainability.
Comprehensive project management solutions covering greenfield, brownfield, and turnkey projects. From initial concept to final handover — end-to-end assistance ensuring on-time, on-budget delivery.
Full range of engineering support services including design assistance for facilities, utilities, clean room panels, AHU systems, and equipment — optimized for performance, safety, and compliance.
Thorough audits to assess your facility's compliance with relevant regulatory standards. We identify potential gaps and provide actionable solutions, minimizing risk and improving performance.
Qualification and validation services for all necessary activities — from equipment qualification to process validation and facility commissioning, ensuring regulatory compliance.
Comprehensive documentation support for your Quality Management System (QMS), ensuring all processes, procedures, and records meet regulatory standards.
Customized training programs designed to boost your team's operational capabilities — covering quality assurance, regulatory compliance, process efficiency, and best practices.
Full preparation for audits and certifications. Our expert team guides you through the process to secure required certifications while maintaining industry compliance.
Expert regulatory navigation — from ensuring compliance with global standards to managing submissions and approvals. We support you in meeting requirements and achieving certification.
Specialized R&D and technology transfer services to help you innovate and scale. Seamless transfer from development to commercial production — accelerating time-to-market.
Innovative software solutions for pharma — batch management, quality control, document management, LIMS, calibration management, and more to streamline operations.
Why PCG
Get In Touch
4781, Block A, Pancham Vihar, Sector 68, Mohali, Punjab, India — 160062
Mon – Sat: 9:00 AM – 5:00 PM
24/7 Virtual Support Available