IMP was established in order to address the industry's arising needs and evolving regulatory environment. IMP provides controlled and monitored packaging and storage areas for reliable packaging of investigational medicinal products and clinical trial related supplies
This facility is GMP certified by the Israeli Ministry of Health and is fully compliant with other relevant regulatory requirements.
It is a separated, access controlled facility for the sole handling of clinical supply, located at SLE premises in Shoham. IMP is easily accessible and allows the customer to adhere to tight schedules and frequent visits.

To schedule a visit in our facility please contact Mrs. Ronnie Rosen at: This email address is being protected from spambots. You need JavaScript enabled to view it.

The facility includes:

  • Receipt area
  • Dedicated rooms for:
    • Primary packaging
    • Secondary packaging
    • Secondary packaging of cytotoxic products
    • Testing and sorting procedure of Printed Packaging Materials (PPMs)

Warehouse area:

Designed to allow segregation for different sponsors/studies /material types and statuses

  • 2 separate sets of warehouses: starting materials and finished products (study kits)
  • Receipt area
  • Separated shipment area
  • Large areas for storage in of starting materials and finished products in various storage conditions
  • Separate refrigerated storage rooms for starting materials and finished products\
  • Retained samples room
  • Returns & rejects room

Who We Are?

A dedicated and professional team which ensures the utmost high level of protocol management to the customer’s satisfaction.
IMP’s team works under strict GMP regulations to assure safe, high-quality and cost-effective product.

Our Management

Ronnie Rosen

BD Director, QP

Limor Teomim

QA Director

Amihay Zolkov

SENIOR Project Manager, QP
Responsible Pharmacist

Yaacov Nimrodi

Warehouse Manager

Orly Mordechay

Planning & Control Manager

Osnat Mamet

QA Auditor

Meet Our Team


We strive to provide our customers high quality, safe and efficient services;
We are committed to meet customer’s requirements and to ensure customer satisfaction with all aspects of the provided services.

Each Investigational Medicinal Product is received/ held/ packaged/ distributed in accordance with the requirements of the investigational product registration file, and in accordance with the requirements of the current Good Manufacturing Practice and current Good Distribution Practice regulations.

IMP management acknowledges that provision of a high quality level of service to their customers, is an essential strategic tool to ensure the continued growth of the company business. Furthermore, the company management is committed to providing the necessary resources for implementation of high level of Quality Management System.