ATP-CGPharm Group

Facility and Process
Engineering

ATP-CGPharm Group has been offering tailor-made solutions for the creation of new facilities as well as for the renovation or extension of existing installations.

What’s inside

Expert Facility & Process Engineering

At ATP-CGPharm, we specialize in designing and optimizing pharmaceutical facilities that meet the highest standards of regulatory compliance and operational efficiency. Whether you’re constructing a new facility or upgrading an existing one, our expert team works with you to provide innovative solutions that streamline your operations and maximize productivity.
Our approach combines technical expertise, industry knowledge, and a deep understanding of regulatory requirements, ensuring your facility is not only compliant but also optimized for maximum efficiency and safety.

Our Facility & Process Engineering Services

Expert Facility & Process Engineering Solutions

We design and coordinate the professional and GMP-compliant implementation of various areas. We offer a range of services designed to support your facility’s design, optimization, and compliance needs. From initial planning to final execution, we ensure that each project meets the highest standards of performance and safety.

Facility Design & Optimization

We design and optimize manufacturing environments that enhance operational efficiency while meeting stringent regulatory standards. Our solutions ensure that every facility is built to maximize space utilization and minimize operational downtime.

Process Engineering & Automation

We apply the latest advancements in process engineering and automation to help pharmaceutical facilities improve workflows and reduce costs. Our solutions are tailored to each facility’s unique needs, ensuring smooth operations and compliance.

GMP Compliance & Regulatory Consulting

Our team provides expert guidance to ensure your facility meets GMP and other regulatory standards. We conduct thorough audits and inspections to identify any gaps and offer solutions that guarantee compliance without compromising efficiency.

Turnkey Solutions

We provide end-to-end services, managing every aspect of your facility project from initial design to final execution. Our turnkey solutions ensure seamless integration of every system and process, reducing the complexity and ensuring smooth transitions.

Why Choose US?

GxP-Compliant Facilities & Processes

The Group offers a broad range of services in GxP engineering, commissioning, qualification validation, quality assurance, quality control and environmental monitoring. ATP-CGPharm Group operates internationally with offices in France and Switzerland. The company has a proven track record of successfully completed projects and is renowned for completing projects in-spec, in-time and in-budget. We plans and realizes your GxP-compliant facilities and processes in the following areas:

Enhanced Product
Quality

GMP compliance ensures that your products meet the highest quality standards, improving consistency and safety while reducing defects and errors in production.

Warehousing
Solutions

Optimizing storage and distribution of pharmaceutical products in compliance with GxP standards.

Quality Control
Laboratories

State-of-the-art facilities for analytical testing and microbiological analysis to ensure product quality and safety.

Research &
Development
Laboratories

Designing R&D spaces that foster innovation while maintaining strict compliance with GxP regulations.

Project Management

Our Typical Project Management in 11 Steps

At ATP-CGPharm, we follow a structured and methodical approach to project management, ensuring that every phase of your facility and process engineering project is carefully executed. Our 11-step process guarantees that we meet your needs with precision, from initial planning to final execution and post-maintenance.

We begin by understanding your needs and assessing the feasibility of the project. This includes evaluating potential challenges, required resources, and timelines to ensure the project is viable.

Our engineering team develops the detailed plans and designs needed for your project. This phase covers all technical aspects, ensuring a solid foundation for execution.

We collaborate with you to establish a clear budget, outlining costs for materials, labor, and additional resources. This step ensures that we stay within financial limits while maintaining quality standards.

We provide the essential engineering plans and documentation required to begin sourcing materials and getting necessary approvals. This includes preparing tender documents to invite bids for the project.

Once the materials are selected, we place orders and manage procurement to ensure that all required items are available on time and meet quality standards.

Our team finalizes the engineering design, confirming that all systems are aligned with regulatory requirements and operational specifications.

We ensure timely delivery of materials to the site and oversee the assembly process. Our experts supervise the installation and construction to guarantee everything is executed according to plan.

We conduct thorough testing to ensure all systems and equipment operate as intended. This includes verifying functionality, safety, and performance under real-world conditions.

Once the project is completed and fully tested, we hand over the facility to you, ensuring everything is in working order and meets your expectations.

We begin by understanding your needs and assessing the feasibility of the project. This includes evaluating potential challenges, required resources, and timelines to ensure the project is viable.

Our engineering team develops the detailed plans and designs needed for your project. This phase covers all technical aspects, ensuring a solid foundation for execution.

We collaborate with you to establish a clear budget, outlining costs for materials, labor, and additional resources. This step ensures that we stay within financial limits while maintaining quality standards.

We provide the essential engineering plans and documentation required to begin sourcing materials and getting necessary approvals. This includes preparing tender documents to invite bids for the project.

Once the materials are selected, we place orders and manage procurement to ensure that all required items are available on time and meet quality standards.

Our team finalizes the engineering design, confirming that all systems are aligned with regulatory requirements and operational specifications.

We ensure timely delivery of materials to the site and oversee the assembly process. Our experts supervise the installation and construction to guarantee everything is executed according to plan.

We conduct thorough testing to ensure all systems and equipment operate as intended. This includes verifying functionality, safety, and performance under real-world conditions.

Once the project is completed and fully tested, we hand over the facility to you, ensuring everything is in working order and meets your expectations.

We perform final qualification and validation to ensure that the facility, equipment, and processes meet all regulatory and operational requirements.

We perform final qualification and validation to ensure that the facility, equipment, and processes meet all regulatory and operational requirements.

We provide ongoing maintenance and support to ensure the facility continues to operate efficiently and remains compliant with all relevant regulations.

Real-World Results

Challenge: The client struggled with manual processes that were time-consuming and prone to errors, affecting product consistency and speed.

Solution: Our team implemented automated solutions for key production processes, including real-time monitoring and data logging systems. We customized the automation to meet the client’s specific needs and ensured that all systems were GMP-compliant.

Outcome: The client saw a 25% increase in production capacity, reduced human error, and improved product quality.

Challenge: The client struggled with manual processes that were time-consuming and prone to errors, affecting product consistency and speed.

Solution: Our team implemented automated solutions for key production processes, including real-time monitoring and data logging systems. We customized the automation to meet the client’s specific needs and ensured that all systems were GMP-compliant.

Outcome: The client saw a 25% increase in production capacity, reduced human error, and improved product quality.

Scroll to Top