X
ACHEMA MIDDLE EAST 2026
Pharma Advancement
DDF Summit 2025
  • Home
  • Articles
  • Drug Development
    • All
    • Clinical Trials
    • FDA Approvals
    • Research & Development
    idiopathic pulmonary fibrosis

    US FDA Approves Jascayd for Idiopathic Pulmonary Fibrosis

    Tissue Repair Drug

    FDA Clears Tissue Repair Drug AD-NP1 For Clinical Trials

    FastTrack Review

    US FDA Launches Fast-Track Review Scheme for Generic Drugs

    AI Based Drug Discovery

    Bristol Myers, Takeda, Astex to Back AI Based Drug Discovery

    wearable drug delivery devices

    Wearable Drug Delivery Devices for On-Demand Care

    biologic drug formulation stability

    Breakthroughs in Biologic Drug Formulation Stability

    high volume injectable formulations

    Overcoming Challenges in High-Volume Injectable Formulations

    lipid nanoparticles in RNA therapies

    Lipid Nanoparticles in RNA and Gene Therapies

    Breast Cancer Therapy

    US FDA Approves Breast Cancer Therapy Inluriyo by Eli Lilly

  • Manufacturing
  • Supply Chain
  • Facilities
  • Insights
  • Events
  • Contact Us
No Result
View All Result
  • Home
  • Articles
  • Drug Development
    • All
    • Clinical Trials
    • FDA Approvals
    • Research & Development
    idiopathic pulmonary fibrosis

    US FDA Approves Jascayd for Idiopathic Pulmonary Fibrosis

    Tissue Repair Drug

    FDA Clears Tissue Repair Drug AD-NP1 For Clinical Trials

    FastTrack Review

    US FDA Launches Fast-Track Review Scheme for Generic Drugs

    AI Based Drug Discovery

    Bristol Myers, Takeda, Astex to Back AI Based Drug Discovery

    wearable drug delivery devices

    Wearable Drug Delivery Devices for On-Demand Care

    biologic drug formulation stability

    Breakthroughs in Biologic Drug Formulation Stability

    high volume injectable formulations

    Overcoming Challenges in High-Volume Injectable Formulations

    lipid nanoparticles in RNA therapies

    Lipid Nanoparticles in RNA and Gene Therapies

    Breast Cancer Therapy

    US FDA Approves Breast Cancer Therapy Inluriyo by Eli Lilly

  • Manufacturing
  • Supply Chain
  • Facilities
  • Insights
  • Events
  • Contact Us
No Result
View All Result
Pharma Advancement
No Result
View All Result
Home Manufacturing

Medivant Launches Pharma Manufacturing operations in US

Content Team by Content Team
11th May 2020
in Manufacturing, News
Medivant Launches Pharma Manufacturing operations in US

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

A new U.S.-based pharmaceutical manufacturer, Tailstorm Health, Inc., DBA Medivant Healthcare, will begin to roll out sterile single dose liquid injectable medications on the FDA’s Drug Shortage List. Medivant’s initial products will include sterile liquid injectables that are in dire need in the ICU for COVID-19 patients.

Throughout the country, hospitals have experienced difficulties receiving orders for more than a dozen sedatives, anesthetics, painkillers, and muscle relaxants, which have been in short supply. Recent reports have shown that orders for these medications are only being filled and shipped to hospitals 53% of the time. Medivant Healthcare said it will quickly fill the needed void and supply hospitals with safe, sterile medications.

Based in Chandler, AZ, Medivant Healthcare is a boutique, cGMP (Current Good Manufacturing Practice) compliant manufacturer, guided by automation that naturally leads to greater output.

Capable of producing 80,000 vials of 1-10 ML single dose liquid injectables per day, Medivant’s facility averages 40,000 vials per shift with a staff of roughly 25 fully-trained professionals. Rollout over the coming year is expected to reach nearly half of the U.S. and their current count of 16 molecules in production will reach 25 plus by 2021.

Medivant Healthcare counts on extensive lineage in the larger pharmaceutical manufacturing world, managed by ownership that dates three generations in pharmaceuticals.

“Over the long-term, Medivant seeks to be a leader in this niche area of hospital drug shortages,” said Viraj Gandhi, owner and director, Medivant. “We are hoping to revive pharmaceutical manufacturing interest in the U.S.”

Medivant serves hospitals, hospital groups, surgical centers, doctors’ offices and emergency centers. It is a business-to-business model with no direct to consumer sales.

Andrew Stasiak, director of quality control, Medivant, said, “As a cGMP manufacturer, safety and quality are paramount and guide all decisions across the organization. Automation has led to little to no human error, and our in-house specialist QA teams work diligently to ensure compliance is met no matter how minute or seemingly insignificant the detail.”

Medivant will immediately begin distributing the following medications to hospital and emergency rooms throughout the U.S.: Lidocane (local anesthetic), Bupivacine (local anesthetic), Ketorolac (non-opioid pain management, Diltiazem (heart medication), Ondansetron (nausea medication), Tramadol (non-opioid pain management), Calcium Chloride (heart medication), Ketamine (C3 pain management, based on licensing approval by DEA), Dextrose (low blood sugar), Metoprofol (heart medication), Ibuprofen (non-opioid pain management), Midazolam (C4 sedative, based on licensing approval by DEA).

Previous Post

Pfizer and BioNTech Dose First Participants in the U.S. as Part of Global COVID-19 mRNA Vaccine Development Program

Next Post

Aptar Submits Application for EUA to the German Regulatory Agency BfArM for ActivShieldTM FFP2 Decontamination System

Related Posts

idiopathic pulmonary fibrosis
Americas

US FDA Approves Jascayd for Idiopathic Pulmonary Fibrosis

9th October 2025
Tissue Repair Drug
Clinical Trials

FDA Clears Tissue Repair Drug AD-NP1 For Clinical Trials

7th October 2025
FastTrack Review
Americas

US FDA Launches Fast-Track Review Scheme for Generic Drugs

7th October 2025
AI Based Drug Discovery
Drug Development

Bristol Myers, Takeda, Astex to Back AI Based Drug Discovery

1st October 2025
API Manufacturing Facility
Americas

AbbVie Launches New API Manufacturing Facility in Illinois

1st October 2025
U.S. manufacturing
Americas

Amgen to Expand U.S. Manufacturing with $650M Investment

30th September 2025
Next Post
Aptar Submits Application for EUA  to the German Regulatory Agency BfArM for ActivShieldTM FFP2 Decontamination System

Aptar Submits Application for EUA to the German Regulatory Agency BfArM for ActivShieldTM FFP2 Decontamination System

Qucik Links

  • Drug Development
  • Manufacturing
  • News
  • Events & Conferences
  • Newsletter Archive
Pharma Advancement

About Us

Pharma Advancement is a leading Pharma information centric website. On one side Pharmaadvancement.com has established itself as one of the most efficient and comprehensive source of Pharma information online, dedicated to providing decision makers in all the Pharma industry sectors with reliable, accurate and useful insights into happenings in the Pharma sector.

Subscribe Us

System

  • Search
  • Sitemap
  • RSS Feed

Resources

  • Advertise with us
  • Contact Us
  • Download Mediapack
  • Newsletters Archive

© 2017 Copyright © Valuemediaservices 2017 All rights reserved.

No Result
View All Result
  • Home
  • Articles
  • Drug Development
  • Manufacturing
  • Supply Chain
  • Facilities
  • Insights
  • Events
  • Contact Us

© 2017 Copyright © Valuemediaservices 2017 All rights reserved.

Login to your account below

Forgotten Password?

Fill the forms bellow to register

All fields are required. Log In

Retrieve your password

Please enter your username or email address to reset your password.

Log In