Trialog Clinical Trials
Trialog Clinical Trials Ltd is the largest and most experienced Clinical Trials Logistics provider in Israel, established in 1999. It offers a comprehensive range of logistics services for clinical trials, including import/export, QP release, storage, distribution, GMP labeling, local sourcing, returns and destructions, decentralized trials, translation services, and more. The company is committed to quality, efficiency, and dependability, serving major multinational pharmaceutical and CRO companies in Israel with a focus on maintaining the integrity of clinical trial materials and supporting the success of clinical research. Additionally, Trialog provides specialized services such as clinical trial logistics for biotech, CDMO, IIS, and other clients, as well as translation and regulatory support.
Industries
Nr. of Employees
small (1-50)
Products
Patient recruitment platform
Platform and campaign services to support patient recruitment and provide access to a patient database for enrollment campaigns.
GMP Labeling
Dedicated GMP department services for primary and secondary relabeling, repackaging, over encapsulation, placebo capsule manufacturing, and kit blinding and randomization.
GMP Labeling Rooms
GMP-certified labeling rooms and activities for clinical trial packaging and labeling services.
Clinical trials logistics and supply chain services
Comprehensive clinical trial logistics services including setup, import and export, storage and distribution under GDP/GMP standards, QP release, and labelling.
Investigator-Initiated Studies (IIS) Logistics Services
Full logistic services for investigator-initiated studies including storage and distribution, GMP labelling, over encapsulation, manufacturing of placebo capsules, and blinding and randomization of kits.
Decentralized trials services DTP/STP
Comprehensive decentralized clinical trial services including home nurse visits, laboratory tests, and direct-to-patient or site-to-patient deliveries.
Patient recruitment platform
Platform and campaign services to support patient recruitment and provide access to a patient database for enrollment campaigns.
GMP Labeling
Dedicated GMP department services for primary and secondary relabeling, repackaging, over encapsulation, placebo capsule manufacturing, and kit blinding and randomization.
GMP Labeling Rooms
GMP-certified labeling rooms and activities for clinical trial packaging and labeling services.
Clinical trials logistics and supply chain services
Comprehensive clinical trial logistics services including setup, import and export, storage and distribution under GDP/GMP standards, QP release, and labelling.
Investigator-Initiated Studies (IIS) Logistics Services
Full logistic services for investigator-initiated studies including storage and distribution, GMP labelling, over encapsulation, manufacturing of placebo capsules, and blinding and randomization of kits.
Decentralized trials services DTP/STP
Comprehensive decentralized clinical trial services including home nurse visits, laboratory tests, and direct-to-patient or site-to-patient deliveries.
Services
Handling import/export regulatory requirements and customs release for clinical trial supplies to enable cross-border study operations.
Local Qualified Person release and regulatory oversight for investigational medicinal products prior to clinical distribution.
Validated GxP-compliant storage across multiple temperature ranges with computerized monitoring, alarms, one-way flow and secured storage for controlled substances.
Nationwide distribution of clinical trial materials to hospitals and clinics using a validated vehicle fleet with temperature control, GPS tracking, dispatch monitoring and delivery confirmation; includes direct-to-patient and same-day delivery options.
GMP-compliant primary and secondary labeling, relabeling, repackaging and secondary manufacturing (including over-encapsulation and placebo production) and blinded kit assembly.
Local procurement of comparator drugs, ancillary supplies and short-term equipment rental to support clinical study timelines.
Handling import/export regulatory requirements and customs release for clinical trial supplies to enable cross-border study operations.
Local Qualified Person release and regulatory oversight for investigational medicinal products prior to clinical distribution.
Validated GxP-compliant storage across multiple temperature ranges with computerized monitoring, alarms, one-way flow and secured storage for controlled substances.
Nationwide distribution of clinical trial materials to hospitals and clinics using a validated vehicle fleet with temperature control, GPS tracking, dispatch monitoring and delivery confirmation; includes direct-to-patient and same-day delivery options.
GMP-compliant primary and secondary labeling, relabeling, repackaging and secondary manufacturing (including over-encapsulation and placebo production) and blinded kit assembly.
Local procurement of comparator drugs, ancillary supplies and short-term equipment rental to support clinical study timelines.
Expertise Areas
- Clinical supply chain management
- Cold-chain and cryogenic logistics
- GMP-compliant secondary packaging and labeling
- Qualified Person (QP) release and regulatory release processes
Key Technologies
- Validated cold-chain transport vehicles
- GPS fleet tracking and dispatch systems
- Computerized temperature logging and alarm systems
- Liquid nitrogen and cryogenic handling systems