From Molecule to Market—Global CMO Made Simple

We help pharmaceutical manufacturers expand globally through regulatory expertise, CMO partnerships, and strategic business development—securing presence in key international markets.

floating molecule
floating molecule
floating molecule

Expertise and execution to help pharmaceutical manufacturers scale across borders with confidence.

Expertise and execution to help pharmaceutical manufacturers scale across borders with confidence.

Expertise and execution to help pharmaceutical manufacturers scale across borders with confidence.

Initial Fit & Market Readiness

Strategic Planning & Partnering

Regulatory & Technical Execution

Go-to-Market Setup

Post-Launch & Lifecycle Support

Scientist wearing safety goggles and blue lab attire, using a pipette to transfer liquid into a vial in a laboratory setting.

We don’t just collect data—we assess your technical readiness, regulatory potential, and commercial fit across global markets. In one step, we determine if you’re ready to scale, and how fast.

Reviewing technical documentation (e.g., existing CTD/eCTD dossiers)

Evaluating facility certifications (EU GMP, WHO PQ, etc.)

Understanding your current export footprint and growth goals

Initial Fit & Market Readiness

Strategic Planning & Partnering

Regulatory & Technical Execution

Go-to-Market Setup

Post-Launch & Lifecycle Support

Scientist wearing safety goggles and blue lab attire, using a pipette to transfer liquid into a vial in a laboratory setting.

We don’t just collect data—we assess your technical readiness, regulatory potential, and commercial fit across global markets. In one step, we determine if you’re ready to scale, and how fast.

Reviewing technical documentation (e.g., existing CTD/eCTD dossiers)

Evaluating facility certifications (EU GMP, WHO PQ, etc.)

Understanding your current export footprint and growth goals

Initial Fit & Market Readiness

Strategic Planning & Partnering

Regulatory & Technical Execution

Go-to-Market Setup

Post-Launch & Lifecycle Support

Scientist wearing safety goggles and blue lab attire, using a pipette to transfer liquid into a vial in a laboratory setting.

We don’t just collect data—we assess your technical readiness, regulatory potential, and commercial fit across global markets. In one step, we determine if you’re ready to scale, and how fast.

Reviewing technical documentation (e.g., existing CTD/eCTD dossiers)

Evaluating facility certifications (EU GMP, WHO PQ, etc.)

Understanding your current export footprint and growth goals

Built for Pharma Manufacturers in China — Engineered for Global Growth Across Regulated Markets

If you have further questions, please reach out via our Contact page.

What does Meditra actually do for pharmaceutical manufacturers?

What does Meditra actually do for pharmaceutical manufacturers?

What does Meditra actually do for pharmaceutical manufacturers?

Does Meditra have experience working with Chinese pharmaceutical manufacturers?

Does Meditra have experience working with Chinese pharmaceutical manufacturers?

Does Meditra have experience working with Chinese pharmaceutical manufacturers?

Which types of products are you focused on?

Which types of products are you focused on?

Which types of products are you focused on?

How does Meditra support international regulatory compliance?

How does Meditra support international regulatory compliance?

How does Meditra support international regulatory compliance?

What kind of commercial partners can you introduce us to?

What kind of commercial partners can you introduce us to?

What kind of commercial partners can you introduce us to?

What happens after market entry? Do you continue supporting us?

What happens after market entry? Do you continue supporting us?

What happens after market entry? Do you continue supporting us?

Going global takes more than GMP—Chinese pharma must overcome strategic, regulatory, and market-entry hurdles to succeed.

Going global takes more than GMP—Chinese pharma must overcome strategic, regulatory, and market-entry hurdles to succeed.

Going global takes more than GMP—Chinese pharma must overcome strategic, regulatory, and market-entry hurdles to succeed.

Chinese pharmaceutical manufacturers have made remarkable strides in scale, efficiency, and technical strength—yet turning domestic production into global commercial success remains a major challenge.

Regulatory Complexity

Adapting to international regulatory frameworks (EMA, FDA, WHO) requires more than translation — it demands a full reengineering of dossiers, GMP alignment, and ICH-compliant stability and QC data.

Regulatory Complexity

Adapting to international regulatory frameworks (EMA, FDA, WHO) requires more than translation — it demands a full reengineering of dossiers, GMP alignment, and ICH-compliant stability and QC data.

Regulatory Complexity

Adapting to international regulatory frameworks (EMA, FDA, WHO) requires more than translation — it demands a full reengineering of dossiers, GMP alignment, and ICH-compliant stability and QC data.

Limited Access to Commercial Channels

Most manufacturers lack established relationships with MA holders, licensing partners, and trusted distributors — making it difficult to commercialize even validated products.

Limited Access to Commercial Channels

Most manufacturers lack established relationships with MA holders, licensing partners, and trusted distributors — making it difficult to commercialize even validated products.

Limited Access to Commercial Channels

Most manufacturers lack established relationships with MA holders, licensing partners, and trusted distributors — making it difficult to commercialize even validated products.

Tech Transfer & Lifecycle Gaps

Bringing a product to market internationally requires much more than production. It involves packaging localization, audit readiness, ongoing variations, and a partner who understands both the language and the landscape.

Tech Transfer & Lifecycle Gaps

Bringing a product to market internationally requires much more than production. It involves packaging localization, audit readiness, ongoing variations, and a partner who understands both the language and the landscape.

Tech Transfer & Lifecycle Gaps

Bringing a product to market internationally requires much more than production. It involves packaging localization, audit readiness, ongoing variations, and a partner who understands both the language and the landscape.

Disclaimer: The challenges and limitations outlined above are based on industry-wide observations and do not reflect the capabilities of any individual company. All information is for general reference and does not constitute regulatory advice.

Smiling man wearing glasses and a pink shirt, showing his arm with a bandage after vaccination.
Smiling man wearing glasses and a pink shirt, showing his arm with a bandage after vaccination.
Smiling man wearing glasses and a pink shirt, showing his arm with a bandage after vaccination.

Why partner with Meditra?

End-to-End Global Expansion Expertise

Meditra isn’t just a consultant — we’re a strategic partner committed to your international success. We manage the entire lifecycle of global expansion for pharmaceutical manufacturers, from initial regulatory strategy and portfolio screening to dossier adaptation, tech transfer coordination, and commercial setup. Our experience spans multiple regulatory systems including EMA, FDA, and WHO, and we’re fluent in transforming domestic assets into globally viable products. Whether you are entering the EU, LATAM, MENA, or prequalified markets, we provide a structured, risk-mitigated approach that accelerates time to market while ensuring full compliance.

Strategic Dual Presence in China and Europe

With operational hubs in both China and Europe, Meditra acts as a true bridge between manufacturing capability and commercial opportunity. Our local teams are embedded in the realities of each side — fluent in the culture, language, and expectations of both manufacturers and regulators. This dual presence allows us to manage cross-border collaboration in real time, handle technical and compliance bottlenecks swiftly, and keep your project moving without costly delays. It also provides you with constant access to a local Meditra team, whether for factory visits, GMP alignment, on-site audits, or European regulatory meetings.

Robust, Built-In Global Commercial Network

Accessing regulated markets isn’t just about having the right product — it’s about having the right relationships. Meditra brings an extensive network of MA holders, distributors, hospital procurement agents, and licensing partners across Europe, LATAM, and the GCC. We leverage these connections to match manufacturers with trusted partners, enabling commercial traction without the long lead times and uncertainty typically associated with market entry. Whether launching under a private label or securing out-licensing deals, our network provides real-world access and speeds up your path to revenue.

Where Molecules Meet Markets.

Where Molecules Meet Markets.

Where Molecules Meet Markets.

Avenida Conflent SN
Pol. Industrial Pomar de Dalt
08916, Badalona
Barcelona, Spain

Email

hello@meditra.eu

Phone

+34 934658452

Built for Market Entry.

MEDITRA HEALTHCARE operates within the European Union and the People’s Republic of China, providing strategic regulatory, commercial, and technical services to pharmaceutical manufacturers and healthcare partners. All activities are conducted in accordance with applicable local and international regulations, including full compliance with the General Data Protection Regulation (GDPR) in Europe.

We are committed to protecting the privacy of all website users and business partners. This website does not permanently store any personal information. Any data collected through contact forms or communication tools is used exclusively to respond to legitimate business inquiries and is processed securely and confidentially. MEDITRA HEALTHCARE does not share, sell, or distribute personal data to third parties without explicit consent.

By using this website, you agree to the terms outlined in this disclaimer and acknowledge our commitment to lawful and responsible data handling across all jurisdictions where we operate.

Avenida Conflent SN
Pol. Industrial Pomar de Dalt
08916, Badalona
Barcelona, Spain

Email

hello@meditra.eu

Phone

+34 934658452

Built for Market Entry.

MEDITRA HEALTHCARE operates within the European Union and the People’s Republic of China, providing strategic regulatory, commercial, and technical services to pharmaceutical manufacturers and healthcare partners. All activities are conducted in accordance with applicable local and international regulations, including full compliance with the General Data Protection Regulation (GDPR) in Europe.

We are committed to protecting the privacy of all website users and business partners. This website does not permanently store any personal information. Any data collected through contact forms or communication tools is used exclusively to respond to legitimate business inquiries and is processed securely and confidentially. MEDITRA HEALTHCARE does not share, sell, or distribute personal data to third parties without explicit consent.

By using this website, you agree to the terms outlined in this disclaimer and acknowledge our commitment to lawful and responsible data handling across all jurisdictions where we operate.

Avenida Conflent SN
Pol. Ind. Pomar de Dalt
08916, Badalona
Barcelona, Spain

Email

hello@meditra.eu

Phone

+34 934658452

Built for Market Entry.

MEDITRA HEALTHCARE operates within the European Union and the People’s Republic of China, providing strategic regulatory, commercial, and technical services to pharmaceutical manufacturers and healthcare partners. All activities are conducted in accordance with applicable local and international regulations, including full compliance with the General Data Protection Regulation (GDPR) in Europe.

We are committed to protecting the privacy of all website users and business partners. This website does not permanently store any personal information. Any data collected through contact forms or communication tools is used exclusively to respond to legitimate business inquiries and is processed securely and confidentially. MEDITRA HEALTHCARE does not share, sell, or distribute personal data to third parties without explicit consent.

By using this website, you agree to the terms outlined in this disclaimer and acknowledge our commitment to lawful and responsible data handling across all jurisdictions where we operate.