Sustainable Facilities, HVAC, and Controlled Environments focuses on pharmaceutical facility design and manufacture, sustainability of pharmaceutical facilities, heating, ventilation, and air conditioning in pharmaceutical facilities, and other aspects of environmental control in pharmaceutical facilities.
Related Guidance Documents
Commissioning & Qualification (1)
Containment (2)
Microbiological & Viral Contamination Control (4)
Supply Chain Management (1)
Sustainable Facilities, HVAC, & Controlled Environments (6)
- Good Practice Guide: Cold Chain Management
- Good Practice Guide: Heating, Ventilation, & Air Conditioning (HVAC)
- Good Practice Guide: Assessing Particulate Containment 2nd Edition
- Good Practice Guide: Containment for Potent Compounds
- Good Practice Guide: Controlled Temperature Chambers 2nd Edition
- Good Practice Guide: HVAC & Process Equipment Air Filters
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Webinars Related to Sustainable Facilities, HVAC & Controlled Environments
iSpeak Blog Posts Related to Sustainable Facilities, HVAC & Controlled Environments
Pharmaceutical Engineering Magazine Articles
Environmental Sustainability in Biopharmaceutical Facility Design
Many emerging tools and technologies support the environmental sustainability of the pharmaceutical…
Case Study: Meeting Manufacturing Needs with a Net Zero Energy Facility
The expected FDA approval for a Treprostinil dry powder inhaler revealed a need for the manufacturer…
Sustainability: Corporate Ambition, Governance, & Accelerated Delivery
The imperative for global action to tackle climate change is clear and the pharmaceutical industry…
Challenges for Net Zero Carbon Pharmaceutical Manufacturing
The scientific community accepts that greenhouse gas (GHG) emissions cause global warming and…
Sustainability Definitions for the Pharmaceutical Industry
While financial investment in novel therapies provides patients with new treatment options and…
Sustainability by Design for Pharmaceutical Products
As the pharmaceutical industry faces ever-changing global challenges and market forces, it must…
![Figure 1: Seasonal comfort (temperature and RH). ©ASHRAE, www.ashrae.org. Used with permission from 2017 ANSI/ASHRAE Standard 55 [4].](/sites/default/files/styles/teaser_image/public/2021-08/0921_PE_SO_TechHaycock_01.jpg?itok=mJiPGN_X)
Temperature & Humidity Requirements in Pharmaceutical Facilities
Defining room temperature and humidity limits is a frequent topic of debate when designing and…
Pharmaceutical Cleanroom Design & ISO 14644-16
Cleanrooms and controlled contamination environments are increasingly being used across many…
Two Real-World Experiences in Global Sustainability
The article appraises the real-world experiences of two pharmaceutical companies approaching the…
Videos Related to Sustainable Facilities, HVAC & Controlled Environments
Training Courses Related To Sustainable Facilities, HVAC & Controlled Environments
GMP Fundamentals: Buildings and Facilities
A “GMP Facility” is a building that is used in the production of pharmaceutical and medical device products. The proper design, layout, function and control of such facilities is essential in the manufacture of pure, safe and effective pharmaceutical products. In this course, learners will focus on understanding the building layout, safety, cleanroom conditions, as well as facility sanitation and ventilation of both production and support areas. In this On Demand course (part 4 of 11), you will learn the elements of GMP Buildings & Facilities, as required by regulation. Interactive Course…
Airflow Pattern Visualization (AFPV)
This Airflow Pattern Visualization online course provides a unique opportunity to explore the requirements for airflow pattern visualization and to see different video examples of actual airflow pattern visualization results. The course provides a comparison of different types of airflow patterns, but focuses primarily on unidirectional airflow patterns in critical areas (ISO 5).
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HVAC & Environmental Control for Life Science Facilities Training Course
This training course focuses on common issues and problems in the operation of a facility and maintaining readiness for cGMP inspection. Topics include control system alarm management, common system construction deficiencies, cGMP documentation, maintaining an "inspection ready" state, frequency of testing and balancing, airflow visualization, air change rate reduction and more.
Concept and Discussion Papers
March / April 2024
Navigating the Asia Pacific Pharmaceutical Landscape for Global Impact Cover: The Asia Pacific…
Pharma 4.0 – Towards IT/OT Architectures for Prescriptive Maintenance
Introduction Faced with global competition and shrinking margins, (bio)pharmaceutical manufacturers…
Process Events for the Life Science Industry - Information Model Concept on OPC UA for Alarms and Audit Trails
Abstract Plug & play in general describes a piece of equipment that is ready to use upon connecting…
January / February 2024
Stakeholders across industries are becoming accustomed to using information technology (IT) systems…
November / December 2023
There is much that large-scale commercial stem cell therapy processes can adopt from the existing…
