Delivering 30 years
of trusted expertise
in nuclear medicine

OUR SERVICES

Discover our complete end-to-end solutions — Tailored to meet your needs

Are you looking to optimize your manufacturing and release costs?
 

Does your intellectual property require end-to-end support, from concept to market?

Are you looking to expand your capacity?
 

cGMP CONTRACT MANUFACTURING & CDMO Services

As a GMP-certified contract development and manufacturing organization (CDMO), we offer end-to-end solutions tailored to the needs of the pharmaceutical and nuclear medicine industries. Our expertise extends the entire development and production lifecycle, ensuring the highest quality and compliance standards.

  • CDMO Services for Liquid & Lyophilized Products – Scalable batch production from 1 to 300 liters
  • Sterile Small-Volume Manufacturing – cGMP-compliant production for clinical trials and R&D
  • API Synthesis – Small molecule API synthesis under strict GMP compliance
  • Drug Product Development – QbD-driven formulation, process development, validation, and scale-up for liquid and lyophilized injections
  • All-Isotope License – Including α-Emitters, supporting a broad range of nuclear medicine applications
  • Comprehensive Tech Transfer & Validation – Covering microbiological, analytical, radioanalytical controls, and stability testing

With a commitment to innovation and excellence, our experienced team provides flexible, scalable, and fully compliant manufacturing solutions to support your development and commercialization needs.

Let’s bring your projects to life—partner with us!

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GLP Contract Research Services – Advancing Innovation in Radiopharmaceuticals

At the forefront of radiopharmaceutical and pharmaceutical research, we provide comprehensive GLP-compliant contract research services to support drug discovery, development, and regulatory compliance.


Preclinical Research & Quality Evaluation

We offer a full suite of research and analytical services to ensure the safety, efficacy, and regulatory readiness of your pharmaceutical innovations.

  • Animal Testing & Biodistribution Studies – In-depth analysis of drug distribution and pharmacokinetics
  • Advanced Imaging Capabilities – Supporting preclinical evaluation with cutting-edge imaging technologies
  • All-Isotope License – Expertise in working with a full range of isotopes, including α-Emitters
  • With a commitment to scientific excellence, precision, and regulatory compliance, our team ensures high-quality research solutions tailored to your project’s needs.
  • Partner with us to bring your pharmaceutical innovations to life.
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QUALITY CONTROL METHOD DEVELOPMENT SERVICES

We are experienced in developing and validating robust, regulatory-compliant analytical methods to support your pharmaceutical products throughout their lifecycle. 
Our Quality Control (QC) Method Development services are designed to meet the highest standards in safety, efficiancy, and consistency.

Analytical and radioanalytical method development and validation (Drug Substance and Drug Product), 

Microbilogical testing (Sterility testing, Endotoxin testing, Identification, PCR)

Animal testing, Biodistribution studies

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GDP-Certified Pharmaceutical Distribution

Reliable. Efficient. European-Centered.

Strategically located in the heart of Europe, we provide GDP-certified, end-to-end distribution services tailored to the unique needs of the pharmaceutical and radiopharmaceutical industries.

Full-Scope Distribution SolutionsFrom product release to warehousing and final delivery, we ensure a seamless and compliant supply chain across the EU.

Pharmaceuticals
Radiopharmaceuticals
Isotope Generators

With robust infrastructure, temperature-controlled logistics, and regulatory expertise, we guarantee safe, timely, and compliant delivery of sensitive products — supporting your business every step of the way.

Your trusted partner in pharmaceutical distribution — throughout Europe and beyond

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Regulatory Services – Seamless Compliance, Expert Guidance

Navigating the complex regulatory landscape is essential for bringing pharmaceutical and radiopharmaceutical products to market. Our comprehensive regulatory services ensure a smooth and efficient approval process, from eCTD preparation to final regulatory approval.

  • End-to-End Regulatory Support – Streamlining the submission and approval process
  • eCTD Preparation & Submission – Ensuring compliance with global regulatory requirements
  • Regulatory Strategy & Consulting – Tailored solutions for pharmaceutical and radiopharmaceutical products

With our expertise, we help you accelerate approvals, ensure compliance, and bring innovations to market faster.

Let us handle the complexities — so you can focus on what matters most.

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