Clinpack is a professional clinical service provider that, in addition to standard activities, offers integrated business support services that make it unique within the sector.

Integrated Business Support Services

EU Regulatory Support

With deep expertise in GDP, GMP, GCP, and relevant EU regulations, we provide proactive, tailored support that empowers our clients to meet their objectives not just compliantly—but with optimal efficiency, cost-effectiveness, and quality.

Strategic Procurement – Proactive Support in Process Planning and Procurement for Smoothly Running Clinical Trials

We empower emerging biotech start-ups with tailored clinical trial sourcing solutions—connecting them with trusted CROs, CMOs/CDMOs, and specialized experts to ensure efficient, compliant, and successful study execution.

Smart VAT Solutions, Full Compliance

We assist with VAT recovery in clinical trials, ensuring full legal compliance – from consulting to execution, with expert involvement in special cases.

Clinical Packaging & Labeling Services

Label design with regulatory support & production

With our expertise and comprehensive services, we optimize and accelerate the labeling process, from initial planning through to final labeling.

Patient kit assembly

Flexible, fast, and GMP compliant — based on the study requirements and client needs, all under 100% quality control.

QP services for clinical trials

ClinPack Ltd. provides certified QP services, Batch certification, release, and consultation services.

Clinical trial logistics, storage, and distribution

IOR/EOR and Customs clearance

These services apply to materials imported from or exported to third countries outside the European Union.

Storage, including Site of Physical Importation, and sample storage

ClinPack ensures 24/7 GDP-compliant, temperature-controlled storage with advanced safety features.

Distribution

Our distribution service ensures fast, temperature-controlled, hand-to-hand delivery using audited couriers and cost-efficient, compliant logistics.

Clinical Supply Services

Comparator, Auxiliary Medicinal Product (AMP), and Ancillary sourcing

ClinPack supports the smooth conduct of clinical trials by sourcing IMPs, AMPs, medical devices, and ancillaries. It also manages the return, storage, and resale of unused supplies remaining after the study completion in case of ancillaries.

Return, Reconciliation, Destruction

ClinPack ensures GCP-compliant full traceability and controlled reconciliation of IMP returns, with certified third-party destruction when needed.

Project and Clinical Supply Management

Our proactive project management ensures timely, cost-effective clinical supply delivery through expert planning, real-time tracking, and agile response to change.

ClinPack was recommended by the CRO as a clinical supply service provider for our Phase II blinded, randomized study conducted in Central Europe. They ensured the seamless importation of 12 pallets of IMD, completed full labelling in a single day, and managed shipments within the required timeframe, quality, and budget. They proactively flagged potential cost increases, and in parallel provided proposals for us to act efficiently contributing to ensure that the study was proceeding as planned. ClinPack is a client-focused, reliable, and professional clinical supply service provider partner.

Sana Alajmovic | Co-Founder & CEO

Sigrid Therapeutics

ClinPack came to our attention in relation to the assembly, storage, and delivery of patient kits required for a Phase II trial conducted in Europe and US. They have executed with precision complemented by their commitment to providing the best value without compromising on quality. With deep professional expertise, a customer-focused approach, and flexibility, ClinPack contributed to the smooth progression of our trial. They are a reliable and professional clinical supply service provider partner that we can always count on.

Asaf Cohen | SVP CMC and Operations

SpliSense

We collaborated with ClinPack in a Phase II double-blind randomized dermatology clinical trial, and they provided the IMP labelling and clinical logistics services. Both parties entered the project as newly established companies, yet this posed no obstacle to effective set-up and collaboration. Throughout the project, ClinPack proved to be a flexible and proactive partner. We greatly appreciated their transparent communication, agile approach and professional commitment to do everything within their means to ensure that the study progressed in line with the planned timelines.

Anfisa Shakhova | Director Business Development

Niche mid-size European CRO

I approached ClinPack with a regulatory question related to the manufacturing activity and authorization of an investigational medicinal product (IMP). Not only did I receive a clear and accurate response, but they also provided valuable guidance on interpreting the relevant regulations and databases. What I particularly appreciated was their prompt support and the fact that they approached the issue from the client’s perspective. Their assistance enabled us not only to stay compliant but also to make the most of the opportunities within the regulatory framework.

Csilla Léka - General manager

Hungarian Clinical Trials - Global Kft.

Clinpack is a professional clinical service provider that, in addition to standard activities, offers integrated business support services that make it unique within the sector.

Here is what our clients are saying about us.