-
Location
-
Asia Pacific
-
Europe
-
Middle East
-
North America
- |
- Contact
- |
-
Currency:Localize your Content
You can set your preferred currency for this account.
Choose a Currency
Currency- CHOOSE YOUR CURRENCY
Update Currency
Changing Currency will cause your current cart to be deleted. Click OK to proceed.
To Keep your current cart, click CLOSE and then save your cart before changing currency.
-
Select Account
Switching accounts will update the product catalog available to you. When switching accounts, your current cart will not move to the new account you select. Your current cart will be available if you log back into this account again.
Account# Account Name City Zip/Post Code CANCELPROCEEDMy Account
-
Location
-
Asia Pacific
-
Europe
-
Middle East
-
North America
- |
- Contact
- |
You are browsing the product catalog for
Why today’s rapidly evolving pharma industry needs advanced building solutions that can keep pace
The pharmaceutical manufacturing industry is undergoing rapid transformation, with new drugs, treatments and therapies promising breakthroughs for disease. Success hinges not just on innovation and technology but also on the facilities where these advancements are developed and produced.
Pharmaceutical buildings must consistently deliver on product quality, safety and regulatory compliance. Facilities must maintain strict control over environmental factors like temperature, humidity and indoor air quality to prevent contamination and safeguard sensitive materials. Moreover, optimizing building performance can be economically beneficial, as enhanced energy efficiency helps reduce operational costs and aligns with the industry’s commitment to sustainability.
The importance of building operations
Pharmaceutical companies operate complex campuses that house various facilities – office buildings, research and development centers, manufacturing plants and quality control sites – as well as intricate processes and equipment. These structures are not merely spaces; they are integral to a safe and compliant manufacturing process. To navigate this complexity, operators require advanced tools that provide visibility into asset performance and enable near real-time monitoring and adjustments. The focus should be on three key steps to achieving operational success:
Step 1: Planning for success
Whether updating an existing facility or constructing a new one, operational efficiency must be a priority to avoid downtime and keep production on schedule. Engaging project partners who understand good manufacturing practices (GMP) is essential. Taking a comprehensive view of overall building performance and integrating systems can help prevent potential issues before they escalate.
This comprehensive view should extend to all operational aspects, including security and climate control, which are critical in pharmaceutical environments. Effective management of HVAC systems is vital to meet GMP standards and maintain indoor air quality, which protects product integrity and maintains safety.
Step 2: Implementing solutions
Achieving operational efficiency relies on deploying sophisticated control systems with redundancy and automated responses. Redundant power and control modules can protect operations during failures, while automated systems minimize downtime by triggering rapid responses when issues arise.
Predictive maintenance is another crucial strategy. Utilizing advanced software controls along with vibration-based sensors to monitor equipment can help detect early warning signs of potential failures, allowing companies to address problems proactively and alleviate the burden on skilled personnel.
Step 3: Complying with regulations
Pharmaceutical companies must be able to demonstrate compliance and quickly identify deviations from standards. Implementing systems that capture and archive data across building operations is essential for accurate audits and regulatory reporting. These systems not only assist in compliance but also enable root-cause analysis of failures, helping prevent future incidents.
Compliance with regulations such as the FDA’s 21 CFR Part 11 requires comprehensive documentation to establish product quality. This validation process is ongoing, necessitating robust measurement and verification. Partnering with the right building solutions provider can help meet these validation requirements by offering the necessary tools and services.
How Honeywell can help
Honeywell has extensive experience supporting pharmaceutical facilities with integrated hardware, software and services essential for operational efficiency to help maximize existing investments.
Unclear what "operational efficiency" means. I think you want to talk about the process (aka supply chain) to get medication to patients
operational efficiency as in anything to improve operations in the building, not just about getting meds out the door, but could improve a research environment or an office space to have better energy use..etc. i think since we speak about it in all of our literature in this way, it's okay to word it this way. let me know if you strongly oppose and we can find a middle ground.
if there is an order to the 4, it should not be "areas"
Contact us today to learn more about how we can help you improve operational efficiency across your pharmaceutical campuses.
Copyright © 2024 Honeywell International Inc.
Maximum File Size
Maximum Files Exceeded
You cannot access this page as this product is not available in your country.
Compare X Products
Clear All
X of 5 products to compare