Drug Production Software Available In Virginia
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Manufactured by Multiply Labs, Inc.based in USA
QCmaestro is Multiply Labs’ automation software. It enables process planning for the robotic systems, and it creates comprehensive digital records for every drug product. QCmaestro is CFR Part 11 compliant, and it works both on-premises and in the cloud. ...
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by N-SIDEbased in BELGIUM
Optimize end-to-end production planning from DS to IMP. The N-SIDE Production App gives you unprecedented flexibility to optimize manufacturing for your clinical projects, from drug substance (DS) to drug product (DP) to investigational medicinal product (IMP). Use the Production ...
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based in USA
Dossplorer™, our advanced cloud-based dossier management solution eliminates manual steps in the exchange of regulatory dossiers and allows you to share, view and review eCTD, NeeS and other dossier formats from any region and access them in any location! Dossplorer™ allows you to share, view and review eCTD, NeeS and other dossier formats from any region and access them from any ...
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by N-SIDEbased in BELGIUM
End-to-end clinical trial supply chain visibility and optimization. Enable ambitious clinical plans through an optimal supply ...
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based in INDIA
A comprehensive and accurate medicine database for different healthcare sectors. Certified database approved by healthcare experts and practitioners. What is a medicine database? To make it short and simple, a medical database has medical information that refers to information such as drugs used to treat a patient caused by some illness or ...
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based in USA
OOS Software to Automate Out of Specification (OOS) Processes to Comply with FDA CGMPs and 21 CFR Part 211 and Part 820 Regulations. In the FDA environment, specifications are essential in maintaining quality. CGMP regulations for finished pharmaceuticals (21 CFR Parts 210-211) and medical devices (21 CFR Part 820) require strict conformance to approved specifications which can be acheived easily ...
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based in USA
Structured Product Labeling (SPL) & Structure Product Monogram (SPM) is the mandatory document markup standard for Regulatory submission of label content, product and facility information, and any subsequent changes to an existing label information in an electronic format. SPL-SPM format defines the structure and content of label ...
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based in USA
The Assure-Trak Compounding Management System ensures patient safety and compliance while driving efficiencies. For the first time, a single system can be deployed covering all compounding across an enterprise. Users can easily produce both sterile and non-sterile compounds through a single platform. The Assure-Trak® Compounding Management System is designed to fulfill the needs of a single ...
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based in USA
Fusion Inhaler Testing (FIT) creates Device Sampling Designs for metered-dose inhalers (MDIs) and dry powder inhalers (DPIs). It supports USP Apparatuses 1–6, Ph.Eur. Apparatuses C, D, and E, and Dose Unit Sampling Apparatuses (DUSAs). FIT also creates coordinated HPLC Testing Designs that are directly exportable to your Chromatography Data Software (CDS) — connectivity includes ...
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