X
Pharma Advancement
  • Home
  • Articles
  • Drug Development
    • All
    • Clinical Trials
    • FDA Approvals
    • Research & Development
    Avadel Pharmaceuticals Receives

    Avadel Pharmaceuticals Receives Orphan Drug Designation from FDA for LUMRYZ™ (sodium oxybate) for Extended-Release Oral Suspension for the Treatment of Idiopathic Hypersomnia

    Robots and AI in Drug

    Robots and AI in Drug Discovery Are Transforming Medicine

    Stringent Policy around COVID Vaccines Laid by FDA

    Stringent Policy around COVID Vaccines Laid by FDA

    Pharmaceutical-Chemicals Market Booms with Rising API Demand

    Pharmaceutical Chemicals Market Booms with Rising API Demand

    Next in Pharma 2025 Innovations

    Next in Pharma 2025: Innovations Shaping the Future

    Work Smart: Go for Hands-Free Lab Informatics at the Bench, Not Scribbled Notes and Delayed Documentation at Your Desk

    Clinical Development

    AI Revolutionizing Drug Discovery and Clinical Development

    Drug-Development

    China’s Super Me-Too Drug Development: A New Pharma Frontier

    Omics Based Clinical Trials

    Asia Pacific Omics-Based Clinical Trials Market Growth

  • Manufacturing
  • Supply Chain
  • Facilities
  • Insights
  • Events
  • Contact Us
No Result
View All Result
  • Home
  • Articles
  • Drug Development
    • All
    • Clinical Trials
    • FDA Approvals
    • Research & Development
    Avadel Pharmaceuticals Receives

    Avadel Pharmaceuticals Receives Orphan Drug Designation from FDA for LUMRYZ™ (sodium oxybate) for Extended-Release Oral Suspension for the Treatment of Idiopathic Hypersomnia

    Robots and AI in Drug

    Robots and AI in Drug Discovery Are Transforming Medicine

    Stringent Policy around COVID Vaccines Laid by FDA

    Stringent Policy around COVID Vaccines Laid by FDA

    Pharmaceutical-Chemicals Market Booms with Rising API Demand

    Pharmaceutical Chemicals Market Booms with Rising API Demand

    Next in Pharma 2025 Innovations

    Next in Pharma 2025: Innovations Shaping the Future

    Work Smart: Go for Hands-Free Lab Informatics at the Bench, Not Scribbled Notes and Delayed Documentation at Your Desk

    Clinical Development

    AI Revolutionizing Drug Discovery and Clinical Development

    Drug-Development

    China’s Super Me-Too Drug Development: A New Pharma Frontier

    Omics Based Clinical Trials

    Asia Pacific Omics-Based Clinical Trials Market Growth

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

Medicine Patient Pool For 2023-25 To Curb Drug Inequalities

Content Team by Content Team
1st February 2023
in Drug Development, News

A novel strategy for 2023–25 adopted by the Medicines Patent Pool looks to lessen the inequalities in access by way of enhancing the affordability as well as availability of health products across low- and-middle-income countries (LMIC).

The MPP which is a public health organization happens to be backed by the United Nations functioning towards a medical access increase and also facilitating the lifesaving medicines development for LMICs.

This organisation looks forward to setting up 10 new licences along with developing 5 fresh products and aiding in 10 tech transfers via its new strategy. Part of this plan includes letting 30 million people get access to MPP-authorised products every year by 2025.

The new strategy will also facilitate the production of required formulations for people who are most vulnerable and support the enhancement of sustainable and diversified manufacturing capacity across low- and-middle-income countries.

Innovative health technologies are another field that MPP wants to drive access to in order to improve the quality of life of people who happen to be living in LMICs and thereby showcase a dip in mortality and morbidity.

5 strategic goals of the MPP strategy for 2023-25

  • Expand the access of innovative drugs particularly for infectious diseases, especially for HIV, viral hepatitis and tuberculosis.
  • Establish voluntary authorization as an impressive access mechanism when it comes to other conditions and ailments, giving a priority to non-communicable diseases, paediatrics, and maternal health.
  • Facilitate the production of and entry into new medical technology, specifically long-acting biologics as well as mRNA vaccines.
  • Accelerate equal access to counteracts for pandemics such as COVID-19 as well as other global health emergencies.
  • Support distinct and sustainable manufacturing capacity for regional and local production technology transfer.

The new strategy is pivotal since, according to MPP, half of the people living in LMICs are still not able to get access to healthcare and required medicines. MPP has gone on to ink 34 licences for numerous technologies related to health and has helped provide access to 30 billion doses pertaining to treatments since 2010. All these numbers have helped define a new strategy.

According to Charles Gore, MPP’s executive director, because of this novel strategy, they are looking to apply this expertise to negotiate and implement authorization and tech transfer contracts to better take care of public health needs.

MPP collaborates with stakeholders at various levels to give importance to and also licence needed medicines and pool intellectual property so as to encourage generic manufacturing and the development of novel formulations. The Swiss Agency for Development and Cooperation has funded the organization’s functions in terms of essential medicine access.

Previous Post

Mettler-Toledo to showcase smart solutions at Interpack which help boost pharma and biopharma manufacturing productivity

Next Post

In-Person Meetings To Begin By The FDA Starting February 13

Related Posts

SCHOTT Pharma Invests
News

SCHOTT Pharma Invests EUR 100 Million in RTU Cartridges

9th June 2025
Avadel Pharmaceuticals Receives
Drug Development

Avadel Pharmaceuticals Receives Orphan Drug Designation from FDA for LUMRYZ™ (sodium oxybate) for Extended-Release Oral Suspension for the Treatment of Idiopathic Hypersomnia

9th June 2025
Robots and AI in Drug
Articles

Robots and AI in Drug Discovery Are Transforming Medicine

29th May 2025
Stringent Policy around COVID Vaccines Laid by FDA
FDA Approvals

Stringent Policy around COVID Vaccines Laid by FDA

29th May 2025
Pharmaceutical-Chemicals Market Booms with Rising API Demand
Asia

Pharmaceutical Chemicals Market Booms with Rising API Demand

28th May 2025
Drugmakers Asked to Strictly Follow the US Pricing Reforms
Manufacturing

Drugmakers Asked to Strictly Follow the US Pricing Reforms

28th May 2025
Next Post

In-Person Meetings To Begin By The FDA Starting February 13

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