PSS Distribution PSS Warehousing & Transportation is the Northeast's premier services provider and a leader in warehousing, storage, transportation and distribution since 1983. PSS is an industry-leading third party distribution services...
Promotech We provide innovative non-personal marketing support services that are essential to the pharmaceutical, health care and life science industries. Through a strong set of core competences, we help you achieve your...
Omnicell Omnicell, Inc., is a leading provider of solutions targeting patient safety and operational efficiency in healthcare facilities. From the point at which a medication arrives at the receiving dock to the time it is...
Accredo Health Group Accredo Health Group, Inc., provides specialized pharmacy and related services for patients with certain complex and chronic conditions.
We offer:
* Specialty retail pharmacy services designed for timely delivery of...
B&C Group B & C Group is a Packaging & Logistics Company solely dedicated to (Pre)Clinical Research. Headquartered in Mont-St-Guibert (South of Brussels), B & C also has an operational site in Moscow (Russia). Our mission is to...
Network Logistics Management As one of America's leading 3rd party providers, we can pickup and deliver virtually any product anywhere in North America. With an on-time record of over 99.5% you can count on your shipment being where you need it, when...
Therapak, Corp. Therapak Corporation is a leading supplier of diagnostic test kits used by hospitals, physicians, laboratories and pharmaceutical companies worldwide. Therapak's quality-driven assembly operation provides a wide range of...
The Food, Drug and Cosmetic Act requires that a drug be the subject of an approved marketing application before it is transported or distributed across state lines. A sponsor however will want to ship an investigational drug to clinical investigators in many states; it must seek an exemption from that legal requirement. The Investigational New Drug Application (IND) obtains this exemption from ...
Shimadzu protein instruments open new avenues to speed biomarkers to the clinic
Discovery Verification Validation Application
Is a patient really sick? What medicine is necessary? In what dosage? Is the patient responding to it? Doctors customarily answer these questions based on a variety of symptoms. But many of the symptoms used today, because of their subjective description and uncertain ...
People who live and breathe maintenance every day are instinctively aware of the benefits of maintenance improvement: lowering costs and increasing output while still remaining compliant. The intent of this paper is to provide a framework for building the formal justification for investing in a CMMS (Computerized Maintenance Management System) or EAM (Enterprise Asset Management) system as part ...
The formulation of drugs into capsules is often utilized in early phase development due to the relatively quicker formulation-development process. The bioavailability of the poorly soluble drugs can be significantly increased when formulated in a solubilized form in a capsule (i.e. liquid or semi-solid filled capsules). Acidic degradation and dyspeptic side effects associated with some compounds ...
UHPLC often provides run times of less than one minute with peak widths of less than 200 milliseconds, which have created challenges for system performance and detection methods. A variety of applications in the pharmaceutical and environmental areas, using small particle columns, is presented to demonstrate the throughput and performance of the new Nexera UHPLC.
The purpose of this white paper is to document and summarize the current status of the regulatory requirements set forth by different agencies like FDA (in US), ICH (in Europe), and that of Japan and China. In the first section of the paper we will provide the background information on the role of FDA, the regulatory agency in the USA, and the current state of cGMP “risk based approach” enforced ...
The voluntary certification of a quality management system, specifically for medical devices, to ISO 13485 proves advantageous, and in many cases essential, for medical companies which export their products in the global market.
In the European Union, the fulfillment of EU Directives (e.g., Active Implantable Medical Device Directive, Medical Device Directive and In Vitro Diagnostic Directive) ...
Pharmaceutical and biotech companies of all sizes are increasingly turning to third parties to execute some or all of their clinical supply activities. There is a need for these companies to control and track these activities in their information systems.
This article addresses the various methods in which the activities of third-party supply contractors and IVRS (Interactive Voice Response ...
Global clinical trial solutions. Real-world results.
The promise of Electronic Data Capture to improve the speed and quality of clinical trials is too great to be ignored. These eight “secrets to success” will help you understand how to fulfill that promise — and gain the full advantage of EDC.
This paper documents a solution provided by DMC to one of its customers in the form of a vision inspection and data acquisition system. DMC is an engineering consulting company that provides custom software solutions for its customers. For this project the customer is a company that operates chemical plating processes for metal products. In this solution, a “smart” digital camera is set up and ...
This webinar introduces Carestream Molecular Imaging's next-generation gel documentation system, the new, fully automated Gel Logic 212 PRO. This system ...
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