European CDMO Delivering Trusted Pharma Solutions with Global Reach

Specializing in development, manufacturing, and regulatory services
for solid and liquid pharmaceutical products

About Us

About

Who We Are

A Science-Driven CDMO With a Global Vision

At Santa Pharm, we are a European-based CDMO with a global focus, committed to providing high-quality pharmaceutical development, manufacturing, and regulatory solutions.

  • End-to-End Product Support: Guiding clients through every stage of the pharmaceutical product lifecycle with tailored solutions.
  • Technical & Regulatory Expertise: Combining deep scientific knowledge with regulatory readiness to ensure smooth and compliant development.
  • Comprehensive Service Offering: From solid dosage and non-sterile liquid formulation to QC testing, batch release, and pharmacovigilance.

Whether you're a biotech start-up or a global pharmaceutical company, we serve as a strategic partner, offering flexible, compliant, and efficient solutions built on transparency, innovation, and scientific integrity.

Years of Experience

Experienced Professionals

Company area in square meters

SERVICES

SERVICES

Our Comprehensive Services Tailored to Your Molecule’s Journey

We provide a full spectrum of pharmaceutical services designed to meet your specific development and commercialization needs

CDMO

We specialize in the development and manufacturing of solid dosage forms such as tablets and capsules, as well as non-sterile liquid formulations including syrups, suspensions, and solutions, utilizing advanced technologies like wet granulation, roller compaction, and direct compression to ensure high-quality, scalable production

EU Batch Testing & Importation

We specialize in seamless EU batch testing and importation, ensuring your medicinal products meet all regulatory standards. From GDP-compliant storage and distribution to expert coordination with logistics partners, we manage every detail. With full traceability and timely market release, we help you navigate EU regulations with confidence and deliver safe, compliant therapies.

Pharmacovigilance Services

Patient safety drives everything we do. Our end-to-end pharmacovigilance solutions go beyond compliance—delivering real-time safety insights and global regulatory alignment. From adverse event tracking to PSURs, signal detection, and risk management plans, we help safeguard your products and your reputation, ensuring trusted, effective therapies stay safe throughout their lifecycle.

Regulatory Services

Turning regulatory complexity into opportunity—that’s our specialty. From flawless CTD/eCTD dossier preparation to managing variations, renewals, GMP audits, and authority interactions, we guide you every step of the way. With deep expertise and proactive strategy, we fast-track approvals, reduce compliance risks, and help you bring safe, effective products to market—faster.

Get in Touch With Us

Let’s bring your next product to life — safely, efficiently, and in full compliance.

Contact Us