Refine by
Locations
- USA
- Alabama
- Alaska
- Arizona
- Arkansas
- California
- Colorado
- Connecticut
- Delaware
- District Of Columbia
- Florida
- Georgia (Us)
- Hawaii
- Idaho
- Illinois
- Indiana
- Iowa
- Kansas
- Kentucky
- Louisiana
- Maine
- Maryland
- Massachusetts
- Michigan
- Minnesota
- Mississippi
- Missouri
- Montana
- Nebraska
- Nevada
- New Hampshire
- New Jersey
- New Mexico
- New York
- North Carolina
- North Dakota
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Vermont
- Virginia
- Washington
- West Virginia
- Wisconsin
- Wyoming
Safety Lancets Instruction Services In Usa
22 services found
by:HingeClinica based inPrinceton, NEW JERSEY (USA)
Our Pharmacovigilance team has global experience in safety reporting in clinical trials and post marketing surveillances. Our team consists of highly educated, professional with medical, pharmacology background and having in-depth knowledge in using various safety databases, safety reporting requirements, Pharmacovigilance regulations and ...
Manufactured by:Von Gahlen Nederland B.V. based inZevenaar, NETHERLANDS
Training and consulting promotes correct use and improves performance. Before delivery, our service engineers provide training to your lab technicians and medical staff about the product and its maintenance. You will also receive a detailed operations and maintenance manual from us that specifies all procedures, safety instructions, maintenance instructions and cleaning ...
Manufactured by:Ortho-Medical GmbH based inDuerbheim, GERMANY
Instruments are a major asset and represent a significant share of the total capital spending of a hospital. The practical experience recorded in this guide, together with a description of fundamental interrelationships, is intended to help users to keep their reusable instruments in good working order and preserve their value for many years, by ensuring proper care and maintenance. It should be ...
Manufactured by:NeuroLogica Corporation based inDanvers, MASSACHUSETTS (USA)
COVID-19 is impacting the daily lives of people across the globe — individuals, families, colleagues, healthcare providers and patients. Amidst these uncertain times, we want to share something you can feel certain about – Samsung NeuroLogica’s unwavering commitment to our employees and customers. Our employees are working harder than ever to ensure a level of service continuity ...
by:Curavit Clinical Research based inBoston, MASSACHUSETTS (USA)
Curavit clinical study teams monitor the trial data in real time to ensure patient safety, protocol adherence and patient retention. incorporates digital consent, telehealth, and remote data capture ...
by:SciShield Inc. based inLebanon, NEW HAMPSHIRE (USA)
Ensuring the continuity of research is especially difficult with the risks and evolving situation related to the COVID-19 pandemic. The ability to effectively put in place new operational plans for research continuity during the pandemic and to show proper due diligence in protecting your researchers is critical to your ability to keep research operations active. However, these new operational ...
by:Emergo by UL based inAustin, TEXAS (USA)
For many healthcare innovators, opportunities to grow can outpace their ability to scale. Building capabilities in-house requires time and resources that many firms don’t have in the evolving commercial and regulatory demands of the healthcare ...
by:Ekotoxikologicke Centrum Bratislava s.r.o. based inBratislava, SLOVAKIA
Ekotox Centers are providing customers support for the cosmetic products registration in EU - Cosmetic Products Safety Assessment, PIF support, CPNP registration and more . The Cosmetics Regulation provides a robust, internationally recognised regime, which reinforces product safety taking into consideration the latest technological developments, including the possible use of nanomaterials. ...
by:OHS Inc. based inCosta Mesa, CALIFORNIA (USA)
Employee drug testing works! Since 1988, “The Drug Testing Index”™ report by Quest Diagnostics Laboratories has been updated and released annually. Their most recent report is based on more than 10 million drug tests of USDOT-regulated, "safety-sensitive", and "general workforce" employees performed during 2021. The success of employee drug testing has long-ago been confirmed! ...
by:Stericycle, Inc. based inLake Forest, ILLINOIS (USA)
A product recall or withdrawal is a source of great anxiety for any manufacturer. Fortunately, Stericycle’s ExpertRECALL can help restore your peace of mind and protect your brand. Whether you are a pharmaceutical, medical device or consumer product manufacturer or retailer, we can handle every aspect of your product recall.Stericycle ExpertRECALL streamlines the entire product recall ...
by:Parsons based inPasadena, VIRGINIA (USA)
An integrated approach for project success Parsons supports its life sciences customers with commissioning, qualifications, and validation needs by routinely performing validation planning for biotechnology, active pharmaceutical ingredients, dosage forms, utilities, and support systems. In addition, our design engineers—in particular, our process engineers, electrical/instrumentation and ...
by:HingeClinica based inPrinceton, NEW JERSEY (USA)
Our clinical operations teams have extensive experience in conduct of multicentric global clinical trials in various therapeutic areas. Our team consists of experienced Clinical Managers, CRAs, Medics, Pharmacologists with excellent medical background and in-depth knowledge on clinical trial regulations and ICH GCP guidelines. We strive to be responsive, flexible and mindful throughout the trial ...
by:Ekotoxikologicke Centrum Bratislava s.r.o. based inBratislava, SLOVAKIA
In the European Union, cosmetics are regulated by the European Commission’s Directorate-General for Internal Market, Industry, Entrepreneurship, and SMEs. The regulation requires that all cosmetic products sold within the European Union must comply with the European Union Cosmetics Regulation (EC) No 1223/2009. The regulation applies to all cosmetics, including hair dyes, perfumes, skin ...
by:Emergo by UL based inAustin, TEXAS (USA)
It is easy to make mistakes in the regulatory process that can delay market entry or incur unnecessary costs. With help from Emergo’s medical device RA/QA consultants, you can pursue the most efficient regulatory route to approval and registration for your device, and maintain compliance with post-market requirements ...
by:Stericycle, Inc. based inLake Forest, ILLINOIS (USA)
Stericycle Sharps Management Service (SMS) has successfully provided safe, environmentally friendly, and cost-effective sharps management services to customers nationwide since 1986. SMS can help customers be compliant and reduce staff exposure to bloodborne ...
by:Product Safety Consulting, Inc. based inBensenville, ILLINOIS (USA)
Careful attention to product compliance and certification are an integral part of the process of developing and marketing medical devices. Certifiers, regulators,and standards-writing bodies such as Underwriters Laboratories (UL), the Canadian Standards Authority, the IEC and the FDA have been working hard to keep up with the pace of change in biotechnology — which has led to a dynamic and ...
by:MMS Holdings Inc. based inCanton, MICHIGAN (USA)
Forward-thinking medical and regulatory writers that produce cohesive, scientifically-accurate, and regulatory-robust ...
Manufactured by:Advanced Energy Industries, Inc. based inDenver, COLORADO (USA)
Shorten product development, increase reliability, and benefit from compliance expertise. Increased lifestyle conditions, patient lifespans, and outpatient procedures are transforming medical equipment. Equipment needs to be more mobile, include data storage and insight capabilities, and be more precise than ever. These requirements drive innovation and make shortened product development cycles ...
by:STEMart based inShirley, CALIFORNIA (USA)
CE marking is the manufacturer's declaration that their product complies technically and administratively with the essential regulatory requirements of Medical Device Directive 93/42/EEC (MDD) and its supplementary Directive 2007/47/EEC, Active Implantable Medical Devices Directive 90/385/EEC (AIMDD) and In Vitro Diagnostics Directive (IVDD) 98/79/EC, which outline the safety and performance ...
by:Auburn Environmental Services (AES) based inHudson, OHIO (USA)
We are committed to supporting the mission of excellence through safety training. In support of this mission, we will ensure that the environment is in balance with all regulatory safety requirements, relevant “community standards” and Institutional resources. This balance is accomplished through specialized training and by implementing controls in the areas of workplace safety and ...