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Who we are

Your Trusted Partner in Pharmaceutical Project Development

 

About MAI CDMO

At MAI CDMO, we help pharmaceutical and biotech companies sort through the complexities of drug development by connecting them with the right contract development and manufacturing organizations (CDMOs) and contract manufacturing organizations (CMOs). Our mission and vision guide us in our commitment to innovation and collaboration.

Our Mission

Transforming the CMO/CDMO market by providing an efficient and user-friendly platform that connects these companies with the pharmaceutical industry. We aim to simplify and expedite the search and contracting process, allowing pharmaceutical companies and manufacturers to focus on what they do best: innovate and grow. We are committed to transparency, quality, and customer satisfaction in all our operations.

   
 

The Vision

To be the world`s leading platform for connecting pharmaceutical projects with development and manufacturing solutions, driving innovation and growth in the sector. We see ourselves as an essential facilitator in the manufacturing ecosystem, helping companies achieve their goals more quickly and efficiently. Our vision is to create a world where finding and contracting the right CMO/CDMO is just one click away.

 

Our Core Values

  1. Collaboration: We believe in building strong partnerships that enhance project success.
  2. Transparency: We prioritize clear communication and honest practices to foster trust.
  3. Science First: Our team comprises professionals from scientific backgrounds—pharmacy, engineering, and medicine—ensuring that scientific rigor is at the heart of everything we do.
  4. Innovation: We aim to introduce more effective and eco-friendly marketing strategies to the industry, promoting sustainable practices.
  5. CMO and CDMO Focus: Our efforts are dedicated to understanding and meeting the unique needs of CMOs, CDMOs, and pharmaceutical companies.

 

Join us at MAI CDMO whether you are a pharmaceutical or biotech company, or a contract manufacturer.

Let us help you achieve your project goals with confidence and efficiency. Together, we can accelerate the delivery of life-changing therapies to patients around the world.

Our Team and Your Trusted Guides

Meet the experts

Álvaro Marcé
Álvaro Marcé

Founder & co-CEO, Pharmacist

Antonio Martínez
Antonio Martínez

Founder & co-CEO, Engineer

Juan Basterra
Juan Basterra

Scientific advisor

Industry News

Check out the latest trends in the contract manufacturing industry

MAI CDMO Launches Website in 5 Languages to Support Global Clients
MAI CDMO Launches Website in 5 Languages to Support Global Clients

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Counting down to CPHI Americas 2025!

2025-05-18

Let’s connect at CPHI Americas

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Practical SEO strategies for CDMOs to increase online visibility and attract pharma and biotech partners.

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WORLD CLASS CONTRACT MANUFACTURERS

Leading CMOs and CDMOs

Italy Europe
 
Aenova Group - Location Latina, Italy
Aenova Group - Location Latina, Italy

Competence Center animal health products and sterile technologies.

Activity: FDF / DRUG PRODUCTS, BIOLOGICS manufacturing

Uses: Investigational, Commercial (Phase IV), Human,...

Services: Regulatory services, Development services,...

Batch Size / Reactor: Small, Medium, Large

Certifications: EMA (EU GMP), FDA (cGMP), ANVISA (Brazil B-GMP),...

Markets: FDA (USA), EMA (EU), ANVISA (Brazil), Russian...

United States North America
 
Cambrex Charles City
Cambrex Charles City

Our 400+ team members in Charles City specialize in late-phase and commercial API development and cGMP manufacturing.

Activity: CHEMICAL-SYNTHETIC manufacturing

Uses: Investigational, Commercial (Phase IV), Human

Services: Development services, Manufacturing services,...

Batch Size / Reactor: Small, Medium, Large

Certifications: EMA (EU GMP), FDA (cGMP), Health Canada (Canada...

Markets: FDA (USA), EMA (EU), PMDA (Japan), Health Canada...

France Europe
 
Cenexi Hérouville Saint Clair
Cenexi Hérouville Saint Clair

The Hérouville-Saint-Clair site, located near Caen, in Normandy, specializes in the manufacture and filling of injectable and non-injectable sterile liquid products. It has a pharmaceutical surface area of 17,900 m2 over 10 hectares and employs 290 people.

Activity: FDF / DRUG PRODUCTS manufacturing

Uses: Investigational, Commercial (Phase IV), Human

Services: Regulatory services, Manufacturing services,...

Batch Size / Reactor: Small, Medium

Certifications: EMA (EU GMP), FDA (cGMP), NMPA (China GMP), ANVISA...

Markets: FDA (USA), EMA (EU), PMDA (Japan), MHRA (UK), TGA...

Spain Europe
 
Grifols International | Barcelona Plant
Grifols International | Barcelona Plant

Sterile manufacturing solutions (small molecules) in flexible bags and vials.

Activity: FDF / DRUG PRODUCTS manufacturing

Uses: Investigational, Commercial (Phase IV), Human,...

Services: Regulatory services, Development services,...

Batch Size / Reactor: Small, Medium, Large

Certifications: ISO, EMA (EU GMP), FDA (cGMP), Health Canada...

Markets: FDA (USA), EMA (EU), PMDA (Japan), Health Canada...

United States North America
 
Lannett CDMO
Lannett CDMO

Lannetts main manufacturing site sits in Seymour, Indiana, and includes capabilities for Oral Solid Dose (OSD) and Liquids.

Activity: FDF / DRUG PRODUCTS manufacturing

Uses: Investigational, Commercial (Phase IV), Human,...

Services: Regulatory services, Development services,...

Batch Size / Reactor: Small, Medium, Large

Certifications: EMA (EU GMP), FDA (cGMP), Health Canada (Canada...

Markets: COFEPRIS (Mexico), FDA (USA), EMA (EU), PMDA...

Switzerland Europe
 
Ophtapharm, a Sentiss Company
Ophtapharm, a Sentiss Company

Ophtalmic and Otic - Solutions, suspensions, emulsions, ointments and gels - FDA Approved facility

Activity: FDF / DRUG PRODUCTS manufacturing

Uses: Investigational, Commercial (Phase IV), Human,...

Services: Regulatory services, Development services,...

Batch Size / Reactor: Small, Medium, Large

Certifications: ISO, EMA (EU GMP), FDA (cGMP), World Health...

Markets: FDA (USA), EMA (EU)

United States North America
 
Pharmaron Coventry Site (US)
Pharmaron Coventry Site (US)

Small Molecule (RSM/APIs) Commercial Facility

Activity: CHEMICAL-SYNTHETIC manufacturing

Uses: Investigational, Commercial (Phase IV), Human,...

Services: Development services, Manufacturing services

Batch Size / Reactor: Small, Medium, Large

Certifications: ISO, FDA (cGMP), ECOVADIS

Markets: FDA (USA), EMA (EU), PMDA (Japan), Health Canada...

Spain Europe
 
VIVUNT PHARMA
VIVUNT PHARMA

CDMO Sterile Oncology Drugs

Activity: FDF / DRUG PRODUCTS manufacturing

Uses: Investigational, Commercial (Phase IV), Human

Services: Manufacturing services, Analytical / QC services,...

Batch Size / Reactor: Small, Medium, Large

Certifications: EMA (EU GMP)

Markets: EMA (EU)

About MAI CDMO

MAI CDMO is a specialized B2B platform designed to assist pharmaceutical and biotechnology companies in navigating the complex landscape of drug development and manufacturing. Our platform is dedicated to facilitating connections between pharmaceutical firms and a diverse network of qualified contract development and manufacturing organizations (CDMOs) and contract manufacturing organizations (CMOs).

Empowering Drug Development

At MAI CDMO, we recognize the multifaceted challenges faced by pharmaceutical companies in bringing innovative therapies to market. Our mission is to simplify this process through our comprehensive platform, which serves as a bridge between your project requirements and the most suitable manufacturing partners.

Our services are structured to meet the specific needs of the pharmaceutical industry. Here are some key features:

  • Comprehensive CDMO and CMO Finder: Our user-friendly platform allows users to efficiently search for and compare a broad range of trusted CMOs and CDMOs, each with demonstrated expertise across various therapeutic areas and dosage forms.

  • Accelerated Clinical Trial Manufacturing: We facilitate the identification of organizations that meet your specific project requirements and timelines, thereby expediting the clinical trial process.

  • Cost Optimization: By streamlining the partner selection process, we enable you to focus on your core development activities while also helping you to optimize manufacturing costs.

Enhancing Visibility for CDMOs and CMOs

MAI CDMO is not just a tool for pharmaceutical companies; we also offer valuable opportunities for CDMOs and CMOs to showcase their capabilities. Our platform is designed to enhance the visibility of these organizations to a targeted audience seeking reliable manufacturing partners.

By joining our network, CMOs and CDMOs can:

  • Increase Industry Visibility: Reach a broader pool of potential clients actively searching for partners with specific skills and experience.

  • Expand Client Acquisition: By displaying their expertise and past successes, organizations can secure new contracts and forge lasting partnerships within the pharmaceutical sector.

  • Streamlined Communication: Our platform offers integrated tools for initial contact, project inquiries, and contract negotiations, facilitating smoother collaboration between pharmaceutical companies and their partners.

Building a Collaborative Pharmaceutical Ecosystem

MAI CDMO is committed to fostering a collaborative environment that encourages innovation and growth within the pharmaceutical development ecosystem. We believe that by connecting pharmaceutical companies with the most qualified CMOs and CDMOs, we can significantly accelerate the development of life-saving therapies for patients worldwide.

Unique Offerings

Our platform goes beyond merely connecting companies; we provide a suite of specialized services to ensure successful partnerships. These services include:

  • Expert Consulting Services: Our team offers free consultation to guide pharmaceutical companies through the CDMO/CMO selection process. We leverage our industry knowledge to help you identify partners who align with your project needs.

  • Data-Driven Insights: We provide valuable insights and analytics to help you understand market trends, supplier capabilities, and competitive pricing. This data empowers you to make informed decisions and foster successful partnerships.

  • Resources and Best Practices: Access a wealth of resources, including articles, case studies, and best practices, to navigate the intricacies of pharmaceutical outsourcing effectively.

Connecting You with the Right Partners

Whether you`re a pharmaceutical company looking to streamline your drug development process or a CDMO seeking to enhance your market presence, MAI CDMO serves as your strategic partner. Our platform is designed to ensure efficient, effective connections that meet the unique demands of the pharmaceutical sector.

In today’s fast-paced pharmaceutical landscape, the ability to quickly find and engage with the right partners is crucial. MAI CDMO is here to provide that vital link. With our advanced tools and resources, you can navigate the complexities of pharmaceutical project development with confidence.

 

Let MAI CDMO help you achieve your pharmaceutical development goals. By connecting you with the right contract manufacturing organizations, we enable you to bring your life-saving therapies to market more efficiently.

Join us today and discover how our innovative platform can drive your success in the global pharmaceutical market.

Contact us

If you have any questions or suggestions, click here. We will be happy to assist you.

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Salvat
VIVUNT
Cambrex
Ascil
Mabion
Lannett