Description.
PharmEng engineers are experienced in building scalable and robust pharmaceutical production facilities and processes while employing state of the art techniques to meet and exceed operational and regulatory requirements. Our experts have successfully completed facility and process engineering projects including; vaccine manufacturing, sterile manufacturing, oral solid and liquid dosage manufacturing, API manufacturing, medical device manufacturing,[…..] […]
Process Validation PharmEng professionals possess experience in validating pharmaceutical and biopharmaceutical manufacturing processes. Our team of experts will prepare necessary protocols incorporating all critical parameters of the process. Execution will incorporate data analysis and resolve any non-conformances. PharmEng will collect and evaluate data to ensure that a process is capable of consistently operating according to[…..] […]
Our experienced PharmEng consultants strive to exceed your project goals and objectives. We understand the importance of developing the most effective and strategic approach that will meet your project schedules and budgets. Our Subject Matter Experts (SME’s) thrive on implementing the latest industry strategies to meet your organizational and regulatory needs, as well as the[…..] […]
Training is an integral part of GMPs. The operations involved in the manufacture of regulated products are highly technical in nature. Inadequate training of personnel can result in products failing to meet the required standards. During inspections, regulatory agencies often find problems related to training programs. PharmEng has been providing training programs to regulated industries[…..] […]
