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Building High-Performance Engineering Teams: A Leader’s Guide 

In the critical field of pharmaceutical manufacturing, where patient safety is paramount, the strength of our engineering teams is not just a matter of efficiency or productivity—it’s a matter of life and death. As leaders, our approach to building and nurturing these teams directly impacts the quality of our output and, ultimately, the safety of […]

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The Evolution and Importance of Building Enclosure Commissioning 

In the realm of construction and building design, the term “commissioning” has grown from a niche concept to a cornerstone of sustainable development. Originally derived from shipbuilding, where commissioning ensured a vessel was ready for sea, building commissioning has adapted to ensure that structures are designed, constructed, and operated to fulfill their intended performances. Particularly, […]

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Navigating the Complexities of LIMS Validation: A Step-by-Step Guide for Pharma and Medical Device Manufacturers 

Laboratory Information Management Systems (LIMS) are pivotal in managing data, improving efficiency, and ensuring compliance in pharmaceutical and medical device manufacturing. However, the process of LIMS validation can be daunting, given its technical and regulatory complexities. This step-by-step guide aims to demystify the process and provide clear guidance for manufacturers.  Step 1: Understanding Regulatory Requirements  […]

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Mastering LEED Commissioning for Sustainable Building

This post serves as a comprehensive guide on LEED commissioning, a vital component in the realm of sustainable building certification. Aimed at both novices and seasoned professionals, it unpacks the nuances of LEED commissioning, underscoring its pivotal role in promoting environmentally responsible, cost-effective construction practices that yield significant social and governance benefits.  LEED stands as […]

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Navigating Winter Cold: Essential Considerations for Temperature Mapping in Storage Facilities 

Temperature mapping is a critical process in temperature-controlled storage facilities, especially during winter. The season’s harsh conditions pose unique challenges that must be meticulously managed to maintain product integrity. This blog delves into the specific challenges of winter temperature mapping and the necessary adjustments to ensure facilities remain compliant and efficient.  1. HVAC Heating Dynamics  […]

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Procuring K- 12 Commissioning in 2024 

In this blog, we aim to assist K-12 capital project teams and owner’s representatives in Washington State by clarifying the commissioning process for school projects. We’ll highlight the differences between the Washington Sustainable Schools Protocol (WSSP) and the Washington State Energy Code, Commercial Provisions (C408), and offer insights for crafting effective Requests for Qualifications (RFQ) […]

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ValGenesis Announces Performance Validation as New Service Partner

ValGenesis Inc., the market leader in enterprise validation lifecycle management systems (VLMS), and Performance Validation, Inc. a 100% employee-owned company serving the life sciences industry since 1988, have partnered to deliver unique compliance-focused digital validation solutions for life sciences companies in the US. Performance Validation is an industry leader with over 30 years of experience […]

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6 Must-Have Qualities in a LIMS Vendor: What You Can’t Afford to Overlook 

Choosing the right Laboratory Information Management System (LIMS) vendor is a critical decision for any pharmaceutical or medical device manufacturing company. The right vendor not only ensures compliance with stringent regulatory standards but also enhances the efficiency and effectiveness of your laboratory operations. Here are six must-have qualities to look for in a LIMS vendor.  […]

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Performance Validation Welcomes Donna Griffith as Director of Technical Services

Performance Validation Welcomes Donna Griffith as Director of Technical Services 

Performance Validation an industry leader with 35 years of experience in analyzing, identifying, and testing the most critical elements of the manufacturing process for FDA-regulated industries is proud to announce the appointment of Donna Griffith as the company’s Director of Technical Services. Donna Griffith brings a wealth of experience and expertise to Performance Validation, having […]

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Optimizing Compliance in Pharma: Navigating Risk-Based CSV for Enhanced GLP Adherence

Computer System Validation (CSV) is crucial for any organization that needs to comply with Good Laboratory Practices (GLPs). GLPs are regulatory quality standards for conducting non-clinical laboratory studies that support the development of products for human or animal health. They require that laboratory data be reliable, consistent, and accurate. To meet these requirements, laboratories that […]

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