Do you have direct relationships with manufacturers?

Yes. We maintain direct relationships with many global manufacturers and qualified distributors. We source as direct as feasible for each project and set up new accounts when needed. We do not publish a list. Availability depends on product status and manufacturer policy.

Can you provide matching placebos?

Often yes. Feasibility depends on formulation, presentation, and legal constraints. We assess options and propose the best route, including matched packaging and labeling where possible.

Do you support Direct to Site and Direct to Patient delivery?

Yes. We deliver to sites in line with protocol and country rules. We support Direct to Patient where allowed and approved by the sponsor and the relevant bodies.

Can you handle controlled substances for trials?

Yes, where licensed and permitted. We store in secure areas, including walk‑in vaults with controlled access, and manage authority interfaces for import and distribution.

Can you support 3rd country import into the EU?

Yes. We coordinate third‑country imports for Investigational Medicinal Products with Qualified Person (QP) oversight and required documentation. Scope depends on product, country, and permits.

Do you supply bulk quantities?

Where appropriate and permitted. We usually optimize batch sizes to match recruitment and reduce waste.

Can you check international availability?

Yes. We perform market availability checks through our affiliate and partner network and provide validated options. Final availability depends on local law and manufacturer policy.

Do you provide labeling?

Yes. We provide study‑specific packaging and labeling, including multilingual content, blinded kits, and country adaptations under GMP‑aligned processes.

Which documents can you provide?

Document availability varies by product and manufacturer. Common items include: * Certificate of Analysis (CoA) * Certificate of Conformity or Compliance (CoC) * EU QP certification or batch release statement * TSE/BSE statements where required * Safety Data Sheet (SDS) * Certificate of Origin and transaction documentation where applicable * Temperature excursion assessment and fit‑for‑use statement (if supported by investigation) * Manufacturer GMP certificate or license * Sterility certificate where relevant * Certificate of a Pharmaceutical Product (CPP) where relevant

Do you manage returns and destruction?

Yes. We handle returns, quarantine, and compliant destruction according to sponsor and regulatory requirements.

What temperature ranges do you support?

Ambient, refrigerated, frozen, and ultra‑cold with validated packaging, monitoring, and excursion management.

What lead times should we plan for?

Lead times vary by product, country, and permits. We provide a project plan with expected timelines after feasibility.

Simplifying Complexity, Enabling Breakthroughs

Clinical trials are complex, fast-moving, and critical to innovation. Komtur delivers integrated supply solutions that support every phase of research—so you can stay focused on science while we handle the rest.

From comparator sourcing and on-demand packaging to regulatory guidance, storage, and site distribution, we ensure precision, compliance, and flexibility—while proactively minimizing risks across the clinical supply chain. With a patient-first mindset and deep experience in local as well as complex multi-national trials, Komtur helps move studies forward safely, reliably, and with confidence.

Comparator Sourcing
Source with confidence. Secure, compliant, and flexible access to comparators from our global network. Delivered with precision and reliability to keep your trial moving without disruption.
Learn more
Packaging and Labeling
Ready when you are. On-demand precision. Custom packaging tailored to study needs, timelines, and local regulations. Ensuring smooth, compliant delivery from site to patient.
Learn more
Storage and Distribution
Always in control. Secure and seamless. Temperature-controlled storage and direct-to-site distribution ensure stability and speed. Flexible models designed for trial realities, whether local or multinational.
Learn more
CT Consulting
Smarter trials through strategic guidance. Expert support to optimize trial supply strategy, forecast demand, and navigate regulatory requirements. This helps you reduce complexity, stay compliant, and accelerate study execution.
Learn more

Why Komtur?

Flexible Comparator Sourcing
A broad supplier network and hybrid sourcing strategies ensure compliant, on-time supply—backed by long-standing, trusted relationships.
Agile Distribution with Local Execution
GDP- and GMP-compliant operations across 18 affiliates enable scalable logistics and direct-to-site delivery in complex trial settings.
Tailored Packaging and Labeling
Custom small-batch packaging and multilingual labeling—adapted to timelines, protocols, and country-specific requirements.
A Heritage of Sponsor Trust
Decades of experience in clinical supply—supporting biotech, big pharma and investigators with precision, reliability, and global coordination.
Regulatory & Strategic Support
Guidance across QP release, IOR services, and import/export compliance—ensuring control, speed, and seamless execution.

“We extend our heartfelt thanks for your exceptional support and dedication, which was crucial to the successful start of our Phase 1 clinical trial..”

Stories our success was built on:

Our expertise and experience are all focused on the same end - enhanced patient experience. Here are just a few of the times we’ve made a difference.

Back from the brink of disaster – twice!

How we saved a Global client’s planning mistake, planned emergency sourcing of a high volume comparator drug from China and exported to Europe.

Shanghai

Read story

Globe

Description

Frequently asked questions

Do you have direct relationships with manufacturers?
Yes. We maintain direct relationships with many global manufacturers and qualified distributors. We source as direct as feasible for each project and set up new accounts when needed. We do not publish a list. Availability depends on product status and manufacturer policy.
Can you provide matching placebos?
Often yes. Feasibility depends on formulation, presentation, and legal constraints. We assess options and propose the best route, including matched packaging and labeling where possible.
Do you support Direct to Site and Direct to Patient delivery?
Yes. We deliver to sites in line with protocol and country rules. We support Direct to Patient where allowed and approved by the sponsor and the relevant bodies.
Can you handle controlled substances for trials?
Yes, where licensed and permitted. We store in secure areas, including walk‑in vaults with controlled access, and manage authority interfaces for import and distribution.
Can you support 3^rd country import into the EU?
Yes. We coordinate third‑country imports for Investigational Medicinal Products with Qualified Person (QP) oversight and required documentation. Scope depends on product, country, and permits.
Do you supply bulk quantities?
Where appropriate and permitted. We usually optimize batch sizes to match recruitment and reduce waste.
Can you check international availability?
Yes. We perform market availability checks through our affiliate and partner network and provide validated options. Final availability depends on local law and manufacturer policy.
Do you provide labeling?
Yes. We provide study‑specific packaging and labeling, including multilingual content, blinded kits, and country adaptations under GMP‑aligned processes.
Which documents can you provide?
Document availability varies by product and manufacturer. Common items include:
- Certificate of Analysis (CoA)
- Certificate of Conformity or Compliance (CoC)
- EU QP certification or batch release statement
- TSE/BSE statements where required
- Safety Data Sheet (SDS)
- Certificate of Origin and transaction documentation where applicable
- Temperature excursion assessment and fit‑for‑use statement (if supported by investigation)
- Manufacturer GMP certificate or license
- Sterility certificate where relevant
- Certificate of a Pharmaceutical Product (CPP) where relevant
Do you manage returns and destruction?
Yes. We handle returns, quarantine, and compliant destruction according to sponsor and regulatory requirements.
What temperature ranges do you support?
Ambient, refrigerated, frozen, and ultra‑cold with validated packaging, monitoring, and excursion management.
What lead times should we plan for?
Lead times vary by product, country, and permits. We provide a project plan with expected timelines after feasibility.

Investigational Medicinal Products (IMP)

Medicinal products or biologics under investigation in clinical trials to assess safety, efficacy, and optimal dosing. This includes investigational treatments, comparators, and placebos used to generate robust clinical evidence prior to approval.

Learn more

Comparators

Approved medicinal products used as reference treatments in clinical trials to benchmark safety and efficacy against investigational therapies.

Learn more

Ancillary Medication

Medicines administered alongside investigational treatments to support patient safety, manage side effects, or meet protocol requirements.

Learn more

Placebo

Inactive products designed to match the investigational or comparator treatment in appearance and administration, supporting unbiased trial design and data integrity.

Learn more

Disease Areas

Disease Areas Text

Hematology
Diseases of blood, bone marrow, and lymphatic systems.

Komtur Service: Trial support, access pathways, and continuity planning ensure reliable treatment availability for benign and malignant disorders.
Cardiology and Metabolic Diseases
Conditions affecting the cardiovascular system and metabolic regulation.

Komtur Service: Supported through access planning, supply continuity, and patient-centric programs combined with market and reimbursement insights to enable long-term treatment adherence.
Neurology
Diseases of the central and peripheral nervous system.

Komtur Service: Specialised access planning and controlled supply models enable continuity of treatment for rare and high-complexity neurological conditions.
Oncology
Malignant diseases across solid and hematologic cancers.

Komtur Service: Comparators, co-medications, early access programs, and hospital onboarding are supported through coordinated, compliant processes.
Endocrinology and Rare Metabolic Diseases
Disorders of endocrine glands and systemic metabolic pathways.

Komtur Service: Tailored access pathways, continuity planning, and patient-centric support ensure reliable long-term treatment for specialised populations.
Infectious Disease
Diseases caused by bacterial, viral, fungal, or parasitic pathogens.

Komtur Service: Rapid sourcing, controlled distribution, and authority-aligned access models support timely treatment and outbreak responsiveness.
Gastroenterology and Hepatology
Diseases of the gastrointestinal tract and hepatobiliary system.

Komtur Service: Site enablement, access planning, and coordinated supply models ensure compliant delivery across acute and chronic care settings.
Pulmonology (Respiratory)
Diseases of the airways and lungs.

Komtur Service: Temperature-controlled supply, access coordination, and device enablement support effective treatment and monitoring.
Dermatology
Diseases of the skin, hair, and nails, including immune-mediated conditions.

Komtur Service: Access coordination, clinic-aligned supply models, and patient support services enable consistent treatment availability and adherence.
Psychiatry and Behavioral Disorders
Conditions affecting cognition, mood, and behavior.

Komtur Service: Controlled access pathways and patient-centric support models enable safe and reliable therapy delivery.
Rheumatology and Orthopedics
Diseases of joints, muscles, bones, and connective tissue.

Komtur Service: Coordinated access pathways and clinic-aligned supply models support continuity of chronic and specialty care.
Urology and Nephrology
Diseases of kidneys, urinary tract, and genitourinary systems.

Komtur Service: Tailored access pathways and continuity-focused support enable compliant treatment across acute and chronic care.
Ophthalmology
Diseases of the eye and visual system.

Komtur Service: Small-batch supply models, precise packaging, and coordinated access planning support compliant treatment delivery.
Otolaryngology and Balance Disorders
Diseases of auditory, vestibular, and upper airway systems.

Komtur Service: Clinic-aligned logistics and continuity planning support reliable delivery across specialised care settings.
Reproductive Medicine and Gynecology
Conditions affecting reproductive and hormonal health.

Komtur Service: Sensitive handling, hospital onboarding, and patient support enable compliant implementation and long-term engagement.
Immunology and Autoimmune Diseases
Chronic immune-mediated and autoimmune conditions.

Komtur Service: Coordinated access pathways, temperature-controlled supply, and patient support programs enable sustained therapy delivery and adherence.
General Medicine and Emergency Care
Therapies used in acute, inpatient, and emergency settings.

Komtur Service: Rapid access models, clinic-fit logistics, and shortage mitigation protect continuity of care in time-critical environments.

Flexible Comparator Sourcing

Agile Distribution with Local Execution

Tailored Packaging and Labeling

A Heritage of Sponsor Trust

Regulatory & Strategic Support

“We extend our heartfelt thanks for your exceptional support and dedication, which was crucial to the successful start of our Phase 1 clinical trial..”

Back from the brink of disaster – twice!

Even when the wheels come off, we find a way to keep your product moving

Do you have direct relationships with manufacturers?

Can you provide matching placebos?

Do you support Direct to Site and Direct to Patient delivery?

Can you handle controlled substances for trials?

Can you support 3rd country import into the EU?

Do you supply bulk quantities?

Can you check international availability?

Do you provide labeling?

Which documents can you provide?

Do you manage returns and destruction?

What temperature ranges do you support?

What lead times should we plan for?

Investigational Medicinal Products (IMP)

Comparators

Ancillary Medication

Placebo

Hematology

Cardiology and Metabolic Diseases

Neurology

Oncology

Endocrinology and Rare Metabolic Diseases

Infectious Disease

Gastroenterology and Hepatology

Pulmonology (Respiratory)

Dermatology

Psychiatry and Behavioral Disorders

Rheumatology and Orthopedics

Urology and Nephrology

Ophthalmology

Otolaryngology and Balance Disorders

Reproductive Medicine and Gynecology

Immunology and Autoimmune Diseases

General Medicine and Emergency Care

Can you support 3^rd country import into the EU?