Aseptic technique is the practice and procedures utilized to prevent contamination from pathogens. There are four main types of aseptic technique, barriers, patient equipment and preparation, environmental controls, and contact guidelines[1]. Each plays an important role in preventing infection.

Barriers protect the patient or product from the transfer of pathogens from personnel, the environment, or both. Some barriers include sterile gloves, sterile gowning, masks, and sterile drapes. A sterile barrier has not touched a contaminated surface.

Sterile equipment and instruments are also utilized. In healthcare, providers will apply cleansing and bacteria-killing preparations to the patient’s skin before a procedure to protect the patient. In pharmaceuticals, sterile forceps, and VHP cycles will be utilized to ensure the manufacturing area is clean.

Environmental controls require maintaining a sterile environment through processes such as keeping doors closed during manufacturing or an operation and keeping the number of individuals in a room at a minimum. Environmental controls can be monitored through environmental monitoring.

Contact guidelines refer to healthcare providers only touching other sterile items once sterile barriers have been placed on. Healthcare providers must avoid touching nonsterile items and surfaces at all costs. The same guidelines apply to sterile devices during pharmaceutical manufacturing.

Aseptic technique is required in the pharmaceutical manufacturing and healthcare industry. If your company needs assistance with its aseptic techniques, EMMA International can assist. Contact us by phone at 248-987-4497 or by email at info@emmainternational.com.


[1] Medical News Today (November, 2018) What is Aseptic Technique?. Retrieved on March 28, 2022 from https://www.medicalnewstoday.com/articles/323615#types

Bano Ahmed

Bano Ahmed

Bano is a Quality Engineer at EMMA International. She has experience in quality control, pharmaceutical and medical device manufacturing, and implementing corrective and preventative actions within the pharmaceutical and medical device industries. Bano has earned a Bachelor of Science in Biology from Pennsylvania State University and a MPH in Population Health Sciences from the University of Michigan.

More Resources

Pattern Recognition as a Quality Superpower

Pattern Recognition as a Quality Superpower

There are always new ways and reasons to apply pattern recognition to quality improvement. Better ensuring patient outcomes in health care facilities and improving accuracy for medical diagnoses are two such frontiers.
Record Control for a Regulated World

Record Control for a Regulated World

In a regulated industry, the prevailing posture of regulatory representatives, in my experience, has been “Show me proof.” In fact, the philosophy I’ve heard repeated by regulators is “If it wasn’t documented, it didn’t happen.”
EU MDR SSCP’s: The Importance of Readability

EU MDR SSCP’s: The Importance of Readability

Among many of the new requirements that EU MDR has introduced, the Summary of Safety and Clinical Performance (SSCP) is certainly one of the more confusing ones for many firms. SSCP’s are required for implantable and Class III devices under EU MDR and is intended to be a public document summarizing important safety and clinical performance information about the device.

Ready to learn more about working with us?

Pin It on Pinterest

Share This