The GMP Group has design and project delivery expertise in all types of secondary manufacturing and packagaing facilities. The GMP Group will take your project from initial sales forecasting to manufacture start-up.
Pharmaceutical manufacturing requires an environment that is designed to meet cGMP standards to ensure the safety, identity, strength, quality, and purity of the product. Product quality assurance and contamination control are key requirements, and The GMP Group brings the skill-set and engineering experience to ensure that your process, utilities and manufacturing space is designed to meet the rigorous demands of an FDA-licensed facility. This is a key requirement for facilities that are designed for drug substance (API) and drug product (fill/finish) manufacturing.
Core capabilities in environment , space design (clean and support areas) process engineering, critical utilities, and GMP equipment engineering provides a foundation for the successful execution of secondary pharmaceutical projects from concept through detailed design. Regardless of whether the goal is to expand an existing facility or to build a new plant, The GMP Group can provide the appropriate solution to meet the business needs.
To speak with us further or to arrange a meeting, please call 08450 344 340 or click below to email us