As the leader in the Healthcare industry, we offer helpful tools such as product videos, interactive webinars, and other resources to help keep your facilities compliant.
This Contec Healthcare webinar explores how the latest USP and NAPRA Model Standards, are reshaping expectations for compounder safety, quality, and operational practices in nonsterile compounding environments.
The Challenge: Compliance with USP chapters <797> and <800> is demanding but patients deserve the best care possible. These chapters describe the conditions, practices and quality standards for compounded sterile preparations (CSPs) made from both non-hazardous and hazardous drugs (HDs).
It is best practice to wipe down surfaces of supplies such as intravenous (IV) bags and vials packaged in cardboard boxes with a disinfectant before bringing the supplies into classified areas of a clean room. Effective decontamination of hazardous drug residues on containers such as IV bags may reduce the risk of occupational exposure. It is critical to understand the risk of penetration of any potential disinfecting or decontaminating agent into the IV bags.
Contec Healthcare provides resources to help healthcare facilities select the right sporicidal agents for controlled environments and cleanrooms. Contact us today.
Unintended exposures to B-lactam antibiotics can lead to severe allergic reactions in susceptible individuals. Guidance from the FDA indicates that manufacturing and compounding operations must minimize the risk of cross-contamination from B-lactam antibiotics by segregation. Analogous to hazardous drug residues, cross contamination of B-lactams also could be reduced by decontamination/deactivation using disinfectants or cleaning agents.
Dive deep into the details of products like critical site wipes, sterile alcohol pads, and the unique features of Contec's offerings. Learn about the changes in cleaning standards and the innovative solutions Contec provides. For more information or to request a visit, head to Contec Healthcare. Don't miss out on these insights! Subscribe for more updates.
Join us live for a 15-minute discussion with industry experts as we prepare for the final 100 days before USP797 becomes official. We will also discuss multiple resources Contec Healthcare is releasing to ensure you are well prepared for November 1st!
With just 50 days left until the revised Chapter 797 goes live, we're here to help you navigate the complexities of sterile supplies management, expiration dates, and BUDs.
Discover the essentials of Contec Healthcare's Essentials HD Spill ToolKit in this informative video. Learn about its USP <800> compliance, clean room-compatible packaging, and (PPE).
Discover Contec Healthcare's Critical Site Wipes in this demo from ASHP 2023. These robust, low-lint wipes are a superior alternative to traditional pads, offering efficient, compliant cleaning.
This webinar provides guidance on managing hazardous drug residue (or referred by NAPRA Model Standards as hazardous contamination), with a focus on NAPRA Model Standards and USP Chapter <800> compliance.
In this Contec Healthcare Cleanovators session, see how USP <795> & <800> intersect, and learn practical, real-world strategies for protecting your team while staying compliant.
This Contec Healthcare Cleanovators session takes USP <800> beyond the checklist. Walk away with bold, actionable strategies that move your practice from compliance to leadership.
In this Contec Healthcare Cleanovators session, apply proven industrial hygiene principles—like temporal and spatial sampling, statistical modeling, and risk-based planning—to help you build a more accurate and defensible sampling program.
This Contec Healthcare Cleanovators Panel focused on addressing key questions from the audience regarding contamination risks in healthcare settings, particularly in relation to hazardous drugs (HDs).
This Contec Healthcare webinar explores how the latest USP and NAPRA Model Standards, are reshaping expectations for compounder safety, quality, and operational practices in nonsterile compounding environments.
Learn more about compounding cell and gene therapies, risk assessments, and how to implement appropriate measures to avoid cross-contamination and occupational exposure in hospital pharmacies.
What happens in Vegas doesn’t stay in Vegas—especially when it comes to sterile compounding best practices. Join clinical support manager Michael Myers and expert panelists George Smith, Annie Lambert, and Dr. Mark Wiencek live from the ASHP Midyear Meeting in Las Vegas as they close out 2025 and look ahead to 2026.
Join Contec's Principal Microbiologist, Dr. Mark Wiencek and Contec Healthcare's Marketing Coordinator, Jodi Cruz, as they discuss the importance of side-by-side customer support.
This expert panel explores the impact of natural disasters on drug supply chains, operational logistics, and patient care while sharing practical mitigation tactics for pharmacies.
Join experts Mary Nazzal and Kate Douglass to explore key issues in the $15B IV therapy industry, focusing on safety, oversight, and compounding practices.
Contec’s Dr. Mark Wiencek joins Vizient, Inc’s VerifiedRx podcast! From CAR-T therapies to viral vectors, cell and gene treatments are reshaping pharmacy practice. Dr. Wiencek, Principal Microbiologist with Contec’s Technical Services Group, shares insights on safely handling these advanced therapies and the real-world challenges facing hospital pharmacies.
Join Contec Healthcare for Cleanovators 2024, a highly interactive discussion by experts in the design, build and maintenance of sterile compounding cleanroom suites. From important elements of initial planning of the physical plant, initial and ongoing certification of the facility as well as the thoughtful development of an effective environmental monitoring plan that verifies the initial and continued working state of microbial control.
Jim Wagner, Principle at Controlled Environment Consulting will share his insights on designing a cleanroom suite that meets or exceeds USP <797> standards through a discussion on important elements such as sink location, ISO classification, HEPA filtered supply airflow, air change rates, room pressures as well as temperature and humidity.
Kyle D Mulder, NSF, CETA SCF, NEBB, CPT CP, the Training and Technical Director at Vanir Technology Group, VTG LLC will put you in the driver’s seat by providing advice on how to become a meaningful participant in your facility’s certification process.
Contec Healthcare shares critical insights on disinfectant best practices amidst COVID-19 concerns. Learn how to safely and effectively use disinfectants from their lead microbiologist in a news segment.
Erin Thane, a pharmaceutical microbiologist and Vice President of Azzur Labs will help listeners understand how to develop a robust environmental monitoring plan that reflects facility design criteria and work practices.
Contec, Inc. has been awarded a Bronze sustainability rating by EcoVadis. Learn more about Contec's Corporate Social Responsibility program at their website.
Join healthcare cleanroom specialists in review questions about ISO classifications, HEPA filter integrity, air sampling, and cleanroom design standards.
Contec, Inc. has received the 2022 Supplier Legacy Award from Premier Inc. for its exceptional customer service and commitment to innovation in healthcar
Explore best practices for residue reduction in compounding pharmacies with our on-demand webinar. Rachel Davidson, Contec Healthcare’s Product Manager, shares expert guidance on residue management to help you comply with USP 797 and USP 800. Access practical insights, advanced residue removal techniques, and a helpful Q&A session.
Learn about our chemistries effective against COVID-19 and similar viruses, and find links to the CDC website and WHO's latest findings. Download the PDF.
Judd Baker, VP of Innovations at Germfree, discusses IV workflow innovations in pharmacy automation. Learn about challenges, solutions, and the integration of technology for safer, more efficient pharmaceutical compounding, emphasizing the importance of modernizing IV workflow to reduce errors and improve patient safety.
CriticalPoint launches new Qualified Person Certification Programs for 503A and 503B Personnel. These national credentialing programs ensure patient safety.
Mary Nazzal and Melanie Dorey, co-owners of Critical Compounding Resources, demonstrate the importance of smoke testing for Primary Engineering Controls (PECs).
A panel of compounding pharmacy experts discuss best practices for transforming hazardous drug (HD) rooms into non-HD environments. Learn about the importance of eliminating HD residues, compliance with health and safety standards, and the effective use of critical site wipes in pharmaceutical settings.
Contec's Peridox RTU is a versatile disinfectant effective against Ebola and other pathogens, as a sporicide, bactericide, virucide, tuberculocide, and fungicide.
Combat C.diff outbreaks with Contec's Peridox RTU, the industry’s fastest sporicidal claim of 3 minutes! Effective against MRSA and more than 40 pathogens.
Abby Roth, microbiologist and owner of Pure Microbiology, shares on cleanroom microbes and the misconceptions surrounding "highly pathogenic organisms" in sterile compounding environments.
Contec, Inc., leading manufacturer of and partner for contamination control products, has released its inaugural Corporate Social Responsibility Report.
Get ready for best practices and ground-breaking insights - our experts are ready to clear the confusion that arises regarding safe handling of materials all the way from your shipping and receiving docks to your cleanroom.
We are pleased to share some exciting news with you. In our commitment to continuously enhance your experience with our products, and provide side-by-side support, we will be updating our branding across all Contec Healthcare product packaging.
Learn how to better understand Safety Data Sheets (SDS) from Contec Healthcare’s panel of experts. Join us on July 20th to discover what to look for on an SDS and how to communicate it effectively to your employees.
Learn about the impact of disinfectants and their residues on stainless steel surfaces. Join us to discover how corrosion happens and how to mitigate it.
Learn best practices for decontamination of hazardous drugs in sterile compounding areas to comply with USP <800> in this informative and fast-paced webinar.
Abby Roth, a leading authority in pharmaceutical microbiology, delivers a transformational presentation tailored specifically for the compounding pharmacy industry with live step-by-step demonstrations.
Director of Inspections for the North Carolina State Board, Krystal Stefanyk, serves as a guide through the essential components of a compounding inspection and the common issues affecting compliance.
Mark Hamm, Director of Oncology Services for Aurora Health Care, explores medication shortages and staffing gaps in pharmacies. With his rich background, including a Doctor of Pharmacy and an MBA, Mark analyzse these critical healthcare challenges and their impact on patient care.
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