Process Plus provides master planning, engineering, design, procurement, construction management and validation services to meet a wide range of pharmaceutical industry applications. Whether you need to engineer a new process or modify an existing one, you can trust our knowledge and technical expertise to support your current projects and prepare you for future operational requirements.
Process Plus has a proven track record in the manufacturing of Active Pharmaceutical Ingredients (API’s), Aseptic Processing, Fill and Finishing, Vial Filling, Tableting, Capsule filling, and Packaging. As technology continually improves, regulations and statutes become more stringent. Process Plus can quickly respond to the dynamic production requirements within a facility undergoing renovation with designs to meet cGMP, FDA, and EMA guidelines and requirements.
You can be confident that Process Plus will work closely with you to design a constructible, safe, and efficient production facility according to your schedule. Our design expertise integrated with our validation process allows you to focus on delivering your products to market on time.