Nowhere is building automation more “mission-critical” than in life-sciences industries, where drug products and medical devices are developed, manufactured, and tested. Today's typical life-sciences campus includes structures as varied as offices, laboratories, animal-care facilities, manufacturing buildings, and warehouses. This article will provide an overview of building-automation requirements in regulated pharmaceutical-manufacturing facilities.

Facilities in which food and drug products for human use are developed, manufactured, tested, or stored must meet the dictates of the U.S. Food and Drug Administration (FDA). Additionally, industry-accepted “good practices” for laboratories, engineering, manufacturing, and automated manufacturing must be followed (Figure 1). These regulations and requirements are in effect throughout the life of a facility, from conceptualization through decommissioning. Failure to comply puts the owner at both regulatory and business risk. For instance, recently, contamination problems at a manufacturing facility resulted in action by both British and U.S. regulators, leading to a significant disruption in the world's supply of flu vaccine.

To minimize such risk, facilities are constructed under a rigorous and well-defined quality-control system. Current engineering and quality-assurance practices relating to facility construction can be found in the International Society for Pharmaceutical Engineering's (ISPE's) “Commissioning and Qualification Baseline Guide”1 (Volume 5 in the ISPE's Baseline Pharmaceutical Engineering Guides series). Practices for automation are addressed in Version 4 of “The Good Automated Manufacturing Practice (GAMP) Guide for Validation of Automated Systems in Pharmaceutical Manufacture” (“GAMP 4”).2


According to “GAMP 4,” the life cycle of a control system for a building-automation system (BAS) serving a production facility starts with the development of a user-requirement specification (URS) (Figure 2). A URS defines what a system is intended to do and what its user's essential needs are. After the URS, a functional specification (FS) is developed. An FS describes what a system will be required to do and what features it must have to meet user requirements. While a URS is general (e.g., “the system must alarm on key parameters”), an FS is detailed (e.g., “each space temperature will require high, low, high-high, and low-low alarms”) and often used as the basis of automation contracts. The successful contractor compiles a detailed design specification (DDS), which, in addition to shop drawings and equipment cut sheets, includes a detailed description of system architecture, hardware, and software integration and how the requirements of both the URS and FS will be met.

Each of these documents is reviewed and approved by the cognizant user, as well as engineering, production, and quality-assurance personnel. And each is critical to the quality-control process, which is defined in the ISPE's “Validation of Process Control Systems” GAMP Good Practice Guide.3

The GAMP quality-assurance process relies on testing at various stages of development. The testing begins with common software modules and is performed in accordance with formalized and approved test protocols. For control-panel hardware, controller software, system servers, and workstations, factory acceptance testing (FAT) generally is required prior to installation. Once the system is installed and connected to the equipment it is intended to control, site acceptance testing (SAT) is conducted.

FAT and SAT protocols and execution typically are the responsibility of the supplier or a third-party commissioning agent and witnessed by a quality-assurance representative of the owner. Final test results are reviewed and approved by the design documents' signatories. The advantage of the FAT and SAT process is that changes required to correct deficiencies can be made “on the fly” as testing progresses, provided they are recorded and design documentation is updated.

The intent of FAT and SAT is to identify and correct problems before a system falls under the watchful eyes of regulators. Once the steps are completed, system “qualification” can begin. The system then falls under “change control.” Identifying and correcting deviations at this stage is costly in terms of delays and schedule slippage, as system software is “locked down.” Each deviation must be brought to the attention of the quality-assurance authority and the proposed remedy reviewed and formally approved.

The “validation” of a control system occurs in three phases:

  • Installation qualification, during which the equipment is verified to match what was approved in the DDS.

  • Operational qualification, during which the system is verified to perform as described in the FS.

  • Performance qualification, during which the system is verified to meet the requirements dictated by the URS.

A “traceability matrix” is maintained throughout the validation process to ensure specification requirements are addressed during design, installation, and testing.

The final quality-assurance requirements to be met before a system is placed into operation include the development and implementation of standard operating procedures (SOPs) and the training of personnel responsible for using and maintaining the system. Typically, SOPs for a BAS concern disaster recovery, backup and archiving, user rights and password assignment, maintenance, and change management.


In drug manufacturing, how space conditions impact the product being made is of primary importance. Space pressurization and volumetric flow rate are controlled to prevent contamination by dirt and pathogens, as well as cross-contamination from the production of other drugs in the facility. Humidity can affect the efficacy and stability of drugs or how effectively they can be pressed into tablets. Temperature can affect production directly or indirectly by fostering the growth of microbial contaminants on workers. Each environmental parameter to be controlled must be evaluated in light of its potential to impact product quality.

In general, fixed-function, configurable controllers, such as those used for variable-air-volume boxes, are not well-suited to pharmaceutical manufacturing because of their inflexibility. Programmable types of controllers are better-suited, with those that can be programmed in a high-level language the best. This is because GAMP holds that all programs be annotated so they can be supported relatively easily throughout the system life cycle. Also, language-based control simplifies the formalized “code-review” process required for most projects involving manufacturing facilities.

Instrument-loop accuracy — the accuracy of a measurement device, plus that of the controller input to which the device is connected — is another chief concern. Because they need to be checked regularly, qualified control instruments should be installed in locations facilitating calibration and maintenance.

Of secondary concern is the selection of field equipment. With some drug products manufactured in hazardous environments, controls must be intrinsically safe or explosion-proof. And with many manufacturing areas subject to washdown, instruments must be able to withstand being deluged with water and cleaning agents. Humidifiers and control valves serving sterile manufacturing areas may need to be made of stainless steel and suitable for clean-in-place sterilization, as the water vapor they disperse into the air may come in contact with the drug product.